Standard Operating Procedures
Standard Operating Procedures
Tzur D. Chemical Procurement. [HTML] [PDF]
Tzur D. Chemical Storage. [HTML] [PDF]
Tzur D. Compound Sample Number. [HTML] [PDF]
Tzur D. Compound Tracking Number. [HTML] [PDF]
Miniaci J. Conducting 'presat' and 'NOESY' 1D Experiments (version 1.1). [HTML] [PDF]
Amegbey G. Conducting 'presat' and 'NOESY' 1D Experiments on Solid Samples (Version 1.0). [HTML] [PDF]
Amegbey G. Conducting 'presat' and 'NOESY' 1D Experiments on Solid Samples (Version 1.1). [HTML] [PDF]
Amegbey G. Dissolution of Standard Samples for NMR Procedure (version 1.0). [HTML] [PDF]
Amegbey G. Dissolution of Standard Samples for NMR Procedure (version 1.1). [HTML] [PDF]
Clements M. Handling Cell Culture (version 1.1). [HTML] [PDF]
Tzur D. How to Ensure Volunteer Information Confidentiality. [HTML] [PDF]
Tzur D. How to Write a Standard Operating Procedure. [HTML] [PDF]
Tzur D. HPLC Standard Operating Procedure A. [HTML] [PDF]
Tzur D. Obtaining Ethics Approval for Human Subjects Samples. [HTML] [PDF]
Tzur D. Obtaining Laboratory Biohazard Certification. [HTML] [PDF]
Tzur D. Obtaining Volunteers Informed Consent. [HTML] [PDF]
Amegbey G. Preparation of NMR Buffers (version 1). [HTML] [PDF]
Tzur D. Sample Analysis by HPLC (version 1). [HTML] [PDF]
Tzur D. Sample Number Tracking for Analysis (version 1). [HTML] [PDF]
Nikolai L. Blood Extraction (version 1). [HTML] [PDF]
Nikolai L. Conducting MS Experiments (version 1). [HTML] [PDF]
Guo N. Conducting MS/MS Experiments (version 1). [HTML] [PDF]
Guo N. Conducting MS/MS Experiments (version 2). [HTML] [PDF]
Guo N. Dissolution of Standard Samples for MS/MS (version 1). [HTML] [PDF]
Nikolai L. Urine Extraction (version 1). [HTML] [PDF]
Maiti R. Protocol for identifying metabolites from biofluids using Chenomx Eclipse NMR software (1D NMR Data). [HTML] [PDF]
Syntheses
Clive DL. Synthesis of N-(2-Furoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryloyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Acryloylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valerylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Propanoylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoylglycine. [HTML] [PDF]
Clive DL. Synthesis of (3-Methylcrotonyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (3-Methylcrotonyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)glycineMethylEster. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of 2-(Benzyloxy)benzoic acid. [HTML] [PDF]
Clive DL. Synthesis of N-[(2-Benzyloxy)benzoyl]glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Hydroxybenzoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelonitrile. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelic acid ethyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelic acid. [HTML] [PDF]
Clive DL. Synthesis of Palmitoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Octanoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Decanoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of (4-Hydroxyphenyl)acetylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (4-Hydroxyphenyl)acetylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyrylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyroylglycine. [HTML] [PDF]
Clive DL. Synthesis of 2-Methylbutyroyl dl-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Hexanoyl dl-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Hexanoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Isovaleryl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Palmitoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of N-Propanoylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Valerylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Acryloylglycine. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxy-2-methylbutyric acid. [HTML] [PDF]
Clive DL. Synthesis of Cyclohex-2-enyl Acetate. [HTML] [PDF]
Clive DL. Synthesis of 2-Acetoxyhexanedioc Acid. [HTML] [PDF]
Clive DL. Synthesis of 2-Hydroxyhexanedioc Acid. [HTML] [PDF]
Clive DL. Synthesis of Isobutyroyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Octanoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of 3-Bromocyclooctene. [HTML] [PDF]
Clive DL. Synthesis of 2-Bromooctanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Octenedioic acid. [HTML] [PDF]
Clive DL. Synthesis of Ethyl 2-Ethyl-3-hydroxypropanoate. [HTML] [PDF]
Clive DL. Synthesis of 2-Ethyl-3-hydroxypropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of Ethyl (±)-3-Hydroxy-2-methylpropanoate. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (S)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-(2,2-Dimethyl-[1,3]dioxolan-4-yl)ethanol. [HTML] [PDF]
Clive DL. Synthesis of (4S)-(2,2-Dimethyl-[1,3]dioxolan-4-yl)acetic acid. [HTML] [PDF]
Clive DL. Synthesis of (2S)-2,3-Dihydroxybutyric acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-Stearoylcarnitine. [HTML] [PDF]
Clive DL. Synthesis of Glutaric acid monomethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutarylglycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutarylglycine. [HTML] [PDF]
Clive DL. Synthesis of Suberylglycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Suberylglycine. [HTML] [PDF]
Clive DL. Synthesis of Octa-1,7-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylpent-4-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Acetoxyhexanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxyhexanedioic acid (3-Hydroxyadipic acid). [HTML] [PDF]
Clive DL. Synthesis of Allyl 2,3,4,6-Tetra-O-benzyl-D-galacto-pyranoside. [HTML] [PDF]
Clive DL. Synthesis of 2,3,4,6-Tetra-O-benzyl-D-galactopyranose. [HTML] [PDF]
Clive DL. Synthesis of 2,3,4,6-Tetra-O-benzyl-D-galactone. [HTML] [PDF]
Clive DL. Synthesis of D-Galactone. [HTML] [PDF]
Clive DL. Synthesis of Sodium Salt of D-Galactonic Acid. [HTML] [PDF]
Clive DL. Synthesis of Trans-4-decenoic acid. [HTML] [PDF]
Clive DL. Synthesis of cis-4-Decenoic acid. [HTML] [PDF]
Clive DL. Synthesis of 1,2-dihydroxycyclooct-5-ene. [HTML] [PDF]
Clive DL. Synthesis of cis-4-octenedial. [HTML] [PDF]
Clive DL. Synthesis of cis-4-octenedioic acid. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglutamic Acid Dimethyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglutamic acid. [HTML] [PDF]
Clive DL. Synthesis of 8-Nonen-2-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-methyloct-7-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 7-Acetoxyoctanoic acid. [HTML] [PDF]
Clive DL. Synthesis of 7-Hydroxyoctanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-(1-Oxopropyl)-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2S,3R)-3-hydroxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2S,3R)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2S,3R)-3-hydroxy-2-methylbutanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2R,3RS)-3-hydroxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2R,3R)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenyl methyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2R,3R)-3-hydroxy-2-methylbutanoic acid. [HTML] [PDF]
Clive DL. Synthesis of 12-[(t-Butyldimethylsilyl)oxy]dodecane-1-ol. [HTML] [PDF]
Clive DL. Synthesis of 12-[(t-Butyldimethylsilyl)oxy]dodecanal. [HTML] [PDF]
Clive DL. Synthesis of 15-[(t-Butyldimethylsilyl)oxy]pentadeca-1-ene-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-[(11-(t-butyldimethylsilyl)oxy]-undecyl]but-3-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxytetradecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxytetradecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 2-methoxy-4-(2-methyl-5-oxooxazol-4-ylidenemethyl)phenyl ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-Vanillactic acid. [HTML] [PDF]
Clive DL. Synthesis of Dodeca-1,11-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylnon-8-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxysebacic acid. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxydecanedioic acid (3-hydroxysebacic acid). [HTML] [PDF]
Clive DL. Synthesis of Deca-1,9-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylhept-6-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Acetoxyoctanedioic acid (3-acetoxysuberic acid). [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxyoctanedioic acid (3-hydroxysuberic acid). [HTML] [PDF]
Clive DL. Synthesis of Ethyl 5-Tetradecenoate. [HTML] [PDF]
Clive DL. Synthesis of 5-Tetradecenoic Acid. [HTML] [PDF]
Clive DL. Synthesis of N-(1-Oxo-3-butenyl)glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of 9-Decenal. [HTML] [PDF]
Clive DL. Synthesis of 1,11-Dodecadiene-3-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-Vinyldec-9-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-2-Acetoxydecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of 2-Hydroxydecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of 1,13-Tetradecadiene-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-(2-Propenyl)undec-10-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxydodecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxydodecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-(1-Oxopropyl)-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-[(2S,3SR)-3-hydroxy-2-methyl-1-oxo-butyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-[(2S,3S)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2S,3S)-3-hydroxy-2-methylbutanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of Isovalerylalanine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of Isovalerylalanine. [HTML] [PDF]
Clive DL. Synthesis of 2,2-D2-Glycine Methyl Ester Hydrochloride. [HTML] [PDF]
Clive DL. Synthesis of Vinylacetyl-2,2,-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valeryl-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valeryl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-[(2-Benzyloxy)benzoyl]-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Hydroxybenzoyl)-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovaleryl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyryl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyroyl-2,2,-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoyl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Glutaryl-2,2-D2-glycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutaryl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Suberyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Suberyl-2,2-D2-glycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Furoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Furoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(4-Hydroxyphenyl)acetyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(4-Hydroxyphenyl)acetyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(acryloyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N- Butyroyl glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N- Hexanoyl glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxaspiro[4.5]dec-8-ylidene)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxa-spiro[4.5]dec-8-yl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxa-spiro[4.5]dec-8-yl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of Trans-(4-Hydroxycyclohexyl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Benzoic Acid 4-(methoxycarbonylmethyl)-cyclohexyl ester. [HTML] [PDF]
Clive DL. Synthesis of Cis-(4-Hydroxycyclohexyl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of Cis-(4-Hydroxycyclohexyl)acetic acid. [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (a). [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (b). [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (c). [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxy-4-methylhexanoic acid. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Oxo-2H-chromen-3-yl)acetamide. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxychromen-2-one. [HTML] [PDF]
Clive DL. Synthesis of (R)-tert-Butyldimethyl(oxiranylmethoxy)silane. [HTML] [PDF]
Clive DL. Synthesis of (2R)-1-(tert-Butyldimethylsilanyloxy)hex-5-en-2-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-(tert-butyldimethylsilanyl-oxymethyl)pent-4-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (R)-2-Acetoxypentanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-2-Hydroxypentanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (3S,5S,6R)-3,5-Dihydroxy-6-hydroxymethyl-tetrahydropyran-2-one. [HTML] [PDF]
Clive DL. Synthesis of (2S,4S,5R)-2,4,5,6-tetrahydroxyhexanoic Acid Sodium Salt. [HTML] [PDF]
Clive DL. Synthesis of N-Boc-l-serine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-2,2-Dimethyloxazolidine-3,4-dicarboxylic acid 3-tert-butyl Ester 4-Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-Hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-Formyl-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-[(1R)-1-Hydroxyhexadec-2-enyl]-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (2S,3R,E)-2-Aminooctadec-4-ene-1,3-diol (d-erythrosphingosine). [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid Chloride. [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid [(1S,2R,E)-2-hydroxy-1-hydroxymethylheptadec-3-enyl)amide. [HTML] [PDF]
Clive DL. Synthesis of (±)-(R*,R*)-1,2-Diphenylethane-1,2-diol. [HTML] [PDF]
Clive DL. Synthesis of (±)-(R*,R*)-5,6-Diphenyl-[1,4]dioxan-2-one. [HTML] [PDF]
Clive DL. Synthesis of (±)-(3S*,5R*,6R*)-3-[(S*)-1-Hydroxypropyl]-5,6-diphenyl[1,4]-dioxan-2-one. [HTML] [PDF]
Clive DL. Synthesis of (±)-(2S*,3S*)-2,3-Dihydroxypantanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (S)-4-Hydroxydihydrofuran-2-one. [HTML] [PDF]
Clive DL. Synthesis of (S)-3,4-Dihydroxybutanoic Acid Lithium Salt. [HTML] [PDF]
Clive DL. Synthesis of (R)-6-Hepten-2-ol. [HTML] [PDF]
Clive DL. Synthesis of (R)-(1-Methylhex-5-enyloxymethyl)benzene. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-(Benzyloxy)hexanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-Hydroxyhexanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-Hydroxyhexanoic Acid Lithium Salt. [HTML] [PDF]
Clive DL. Synthesis of D-(+)-1,2:5,6-Di-O-isopropylidenemannitol. [HTML] [PDF]
Clive DL. Synthesis of (R)-2,2-Dimethyl[1,3]dioxolane-4-carbaldehyde. [HTML] [PDF]
Tzur D. Chemical Procurement. [HTML] [PDF]
Tzur D. Chemical Storage. [HTML] [PDF]
Tzur D. Compound Sample Number. [HTML] [PDF]
Tzur D. Compound Tracking Number. [HTML] [PDF]
Miniaci J. Conducting 'presat' and 'NOESY' 1D Experiments (version 1.1). [HTML] [PDF]
Amegbey G. Conducting 'presat' and 'NOESY' 1D Experiments on Solid Samples (Version 1.0). [HTML] [PDF]
Amegbey G. Conducting 'presat' and 'NOESY' 1D Experiments on Solid Samples (Version 1.1). [HTML] [PDF]
Amegbey G. Dissolution of Standard Samples for NMR Procedure (version 1.0). [HTML] [PDF]
Amegbey G. Dissolution of Standard Samples for NMR Procedure (version 1.1). [HTML] [PDF]
Clements M. Handling Cell Culture (version 1.1). [HTML] [PDF]
Tzur D. How to Ensure Volunteer Information Confidentiality. [HTML] [PDF]
Tzur D. How to Write a Standard Operating Procedure. [HTML] [PDF]
Tzur D. HPLC Standard Operating Procedure A. [HTML] [PDF]
Tzur D. Obtaining Ethics Approval for Human Subjects Samples. [HTML] [PDF]
Tzur D. Obtaining Laboratory Biohazard Certification. [HTML] [PDF]
Tzur D. Obtaining Volunteers Informed Consent. [HTML] [PDF]
Amegbey G. Preparation of NMR Buffers (version 1). [HTML] [PDF]
Tzur D. Sample Analysis by HPLC (version 1). [HTML] [PDF]
Tzur D. Sample Number Tracking for Analysis (version 1). [HTML] [PDF]
Nikolai L. Blood Extraction (version 1). [HTML] [PDF]
Nikolai L. Conducting MS Experiments (version 1). [HTML] [PDF]
Guo N. Conducting MS/MS Experiments (version 1). [HTML] [PDF]
Guo N. Conducting MS/MS Experiments (version 2). [HTML] [PDF]
Guo N. Dissolution of Standard Samples for MS/MS (version 1). [HTML] [PDF]
Nikolai L. Urine Extraction (version 1). [HTML] [PDF]
Maiti R. Protocol for identifying metabolites from biofluids using Chenomx Eclipse NMR software (1D NMR Data). [HTML] [PDF]
Syntheses
Clive DL. Synthesis of N-(2-Furoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryloyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Acryloylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valerylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Propanoylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoylglycine. [HTML] [PDF]
Clive DL. Synthesis of (3-Methylcrotonyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (3-Methylcrotonyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)glycineMethylEster. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of 2-(Benzyloxy)benzoic acid. [HTML] [PDF]
Clive DL. Synthesis of N-[(2-Benzyloxy)benzoyl]glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Hydroxybenzoyl)glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelonitrile. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelic acid ethyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxymandelic acid. [HTML] [PDF]
Clive DL. Synthesis of Palmitoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Octanoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Decanoyl (±)-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of (4-Hydroxyphenyl)acetylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (4-Hydroxyphenyl)acetylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyrylglycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyroylglycine. [HTML] [PDF]
Clive DL. Synthesis of 2-Methylbutyroyl dl-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Hexanoyl dl-Carnitine Chloride. [HTML] [PDF]
Clive DL. Synthesis of Hexanoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Isovaleryl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Palmitoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of N-Propanoylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Valerylglycine. [HTML] [PDF]
Clive DL. Synthesis of N-Acryloylglycine. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxy-2-methylbutyric acid. [HTML] [PDF]
Clive DL. Synthesis of Cyclohex-2-enyl Acetate. [HTML] [PDF]
Clive DL. Synthesis of 2-Acetoxyhexanedioc Acid. [HTML] [PDF]
Clive DL. Synthesis of 2-Hydroxyhexanedioc Acid. [HTML] [PDF]
Clive DL. Synthesis of Isobutyroyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of Octanoyl l-Carnitine. [HTML] [PDF]
Clive DL. Synthesis of 3-Bromocyclooctene. [HTML] [PDF]
Clive DL. Synthesis of 2-Bromooctanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Octenedioic acid. [HTML] [PDF]
Clive DL. Synthesis of Ethyl 2-Ethyl-3-hydroxypropanoate. [HTML] [PDF]
Clive DL. Synthesis of 2-Ethyl-3-hydroxypropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of Ethyl (±)-3-Hydroxy-2-methylpropanoate. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (S)-3-Hydroxy-2-methylpropanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-(2,2-Dimethyl-[1,3]dioxolan-4-yl)ethanol. [HTML] [PDF]
Clive DL. Synthesis of (4S)-(2,2-Dimethyl-[1,3]dioxolan-4-yl)acetic acid. [HTML] [PDF]
Clive DL. Synthesis of (2S)-2,3-Dihydroxybutyric acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-Stearoylcarnitine. [HTML] [PDF]
Clive DL. Synthesis of Glutaric acid monomethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutarylglycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutarylglycine. [HTML] [PDF]
Clive DL. Synthesis of Suberylglycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Suberylglycine. [HTML] [PDF]
Clive DL. Synthesis of Octa-1,7-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylpent-4-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Acetoxyhexanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxyhexanedioic acid (3-Hydroxyadipic acid). [HTML] [PDF]
Clive DL. Synthesis of Allyl 2,3,4,6-Tetra-O-benzyl-D-galacto-pyranoside. [HTML] [PDF]
Clive DL. Synthesis of 2,3,4,6-Tetra-O-benzyl-D-galactopyranose. [HTML] [PDF]
Clive DL. Synthesis of 2,3,4,6-Tetra-O-benzyl-D-galactone. [HTML] [PDF]
Clive DL. Synthesis of D-Galactone. [HTML] [PDF]
Clive DL. Synthesis of Sodium Salt of D-Galactonic Acid. [HTML] [PDF]
Clive DL. Synthesis of Trans-4-decenoic acid. [HTML] [PDF]
Clive DL. Synthesis of cis-4-Decenoic acid. [HTML] [PDF]
Clive DL. Synthesis of 1,2-dihydroxycyclooct-5-ene. [HTML] [PDF]
Clive DL. Synthesis of cis-4-octenedial. [HTML] [PDF]
Clive DL. Synthesis of cis-4-octenedioic acid. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglutamic Acid Dimethyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovalerylglutamic acid. [HTML] [PDF]
Clive DL. Synthesis of 8-Nonen-2-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-methyloct-7-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 7-Acetoxyoctanoic acid. [HTML] [PDF]
Clive DL. Synthesis of 7-Hydroxyoctanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-(1-Oxopropyl)-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2S,3R)-3-hydroxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2S,3R)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2S,3R)-3-hydroxy-2-methylbutanoic acid. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2R,3RS)-3-hydroxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4S)-3-[(2R,3R)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenyl methyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2R,3R)-3-hydroxy-2-methylbutanoic acid. [HTML] [PDF]
Clive DL. Synthesis of 12-[(t-Butyldimethylsilyl)oxy]dodecane-1-ol. [HTML] [PDF]
Clive DL. Synthesis of 12-[(t-Butyldimethylsilyl)oxy]dodecanal. [HTML] [PDF]
Clive DL. Synthesis of 15-[(t-Butyldimethylsilyl)oxy]pentadeca-1-ene-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-[(11-(t-butyldimethylsilyl)oxy]-undecyl]but-3-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxytetradecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxytetradecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 2-methoxy-4-(2-methyl-5-oxooxazol-4-ylidenemethyl)phenyl ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-Vanillactic acid. [HTML] [PDF]
Clive DL. Synthesis of Dodeca-1,11-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylnon-8-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxysebacic acid. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxydecanedioic acid (3-hydroxysebacic acid). [HTML] [PDF]
Clive DL. Synthesis of Deca-1,9-dien-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-allylhept-6-enyl ester. [HTML] [PDF]
Clive DL. Synthesis of 3-Acetoxyoctanedioic acid (3-acetoxysuberic acid). [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxyoctanedioic acid (3-hydroxysuberic acid). [HTML] [PDF]
Clive DL. Synthesis of Ethyl 5-Tetradecenoate. [HTML] [PDF]
Clive DL. Synthesis of 5-Tetradecenoic Acid. [HTML] [PDF]
Clive DL. Synthesis of N-(1-Oxo-3-butenyl)glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of 9-Decenal. [HTML] [PDF]
Clive DL. Synthesis of 1,11-Dodecadiene-3-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-Vinyldec-9-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-2-Acetoxydecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of 2-Hydroxydecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of 1,13-Tetradecadiene-4-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic Acid 1-(2-Propenyl)undec-10-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Acetoxydodecanedioic acid. [HTML] [PDF]
Clive DL. Synthesis of (±)-3-Hydroxydodecanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-(1-Oxopropyl)-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-[(2S,3SR)-3-hydroxy-2-methyl-1-oxo-butyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (4R)-3-[(2S,3S)-3-acetoxy-2-methyl-1-oxobutyl]-4-(phenylmethyl)-2-oxazolidinone. [HTML] [PDF]
Clive DL. Synthesis of (2S,3S)-3-hydroxy-2-methylbutanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of Isovalerylalanine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of Isovalerylalanine. [HTML] [PDF]
Clive DL. Synthesis of 2,2-D2-Glycine Methyl Ester Hydrochloride. [HTML] [PDF]
Clive DL. Synthesis of Vinylacetyl-2,2,-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valeryl-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Valeryl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-[(2-Benzyloxy)benzoyl]-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Hydroxybenzoyl)-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Isovaleryl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyryl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-isobutyroyl-2,2,-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoyl-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-Hexanoyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)-2,2-D2-glycine Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methylbutyroyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(3-Phenylpropionyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Glutaryl-2,2-D2-glycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of Glutaryl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Suberyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of Suberyl-2,2-D2-glycine dimethyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Furoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Furoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Methoxybenzoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Phenylacetyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryoyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(Methacryoyl)-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-(4-Hydroxyphenyl)acetyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(4-Hydroxyphenyl)acetyl-2,2-D2-glycine. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-Butyroyl-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N-(acryloyl)-2,2-D2-glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N- Butyroyl glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of N- Hexanoyl glycine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxaspiro[4.5]dec-8-ylidene)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxa-spiro[4.5]dec-8-yl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (1,4-Dioxa-spiro[4.5]dec-8-yl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of Trans-(4-Hydroxycyclohexyl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Benzoic Acid 4-(methoxycarbonylmethyl)-cyclohexyl ester. [HTML] [PDF]
Clive DL. Synthesis of Cis-(4-Hydroxycyclohexyl)acetic acid methyl ester. [HTML] [PDF]
Clive DL. Synthesis of Cis-(4-Hydroxycyclohexyl)acetic acid. [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (a). [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (b). [HTML] [PDF]
Clive DL. Synthesis of (E)-2-Meethylpent-2-enedioc acid (c). [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxy-4-methylhexanoic acid. [HTML] [PDF]
Clive DL. Synthesis of N-(2-Oxo-2H-chromen-3-yl)acetamide. [HTML] [PDF]
Clive DL. Synthesis of 3-Hydroxychromen-2-one. [HTML] [PDF]
Clive DL. Synthesis of (R)-tert-Butyldimethyl(oxiranylmethoxy)silane. [HTML] [PDF]
Clive DL. Synthesis of (2R)-1-(tert-Butyldimethylsilanyloxy)hex-5-en-2-ol. [HTML] [PDF]
Clive DL. Synthesis of Acetic acid 1-(tert-butyldimethylsilanyl-oxymethyl)pent-4-enyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (R)-2-Acetoxypentanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-2-Hydroxypentanedioic Acid. [HTML] [PDF]
Clive DL. Synthesis of (3S,5S,6R)-3,5-Dihydroxy-6-hydroxymethyl-tetrahydropyran-2-one. [HTML] [PDF]
Clive DL. Synthesis of (2S,4S,5R)-2,4,5,6-tetrahydroxyhexanoic Acid Sodium Salt. [HTML] [PDF]
Clive DL. Synthesis of N-Boc-l-serine methyl ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-2,2-Dimethyloxazolidine-3,4-dicarboxylic acid 3-tert-butyl Ester 4-Methyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-Hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-Formyl-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (4S)-4-[(1R)-1-Hydroxyhexadec-2-enyl]-2,2-dimethyloxazolidine-3-carboxylic Acid tert-Butyl Ester. [HTML] [PDF]
Clive DL. Synthesis of (2S,3R,E)-2-Aminooctadec-4-ene-1,3-diol (d-erythrosphingosine). [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid Chloride. [HTML] [PDF]
Clive DL. Synthesis of Tricosanoic Acid [(1S,2R,E)-2-hydroxy-1-hydroxymethylheptadec-3-enyl)amide. [HTML] [PDF]
Clive DL. Synthesis of (±)-(R*,R*)-1,2-Diphenylethane-1,2-diol. [HTML] [PDF]
Clive DL. Synthesis of (±)-(R*,R*)-5,6-Diphenyl-[1,4]dioxan-2-one. [HTML] [PDF]
Clive DL. Synthesis of (±)-(3S*,5R*,6R*)-3-[(S*)-1-Hydroxypropyl]-5,6-diphenyl[1,4]-dioxan-2-one. [HTML] [PDF]
Clive DL. Synthesis of (±)-(2S*,3S*)-2,3-Dihydroxypantanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (S)-4-Hydroxydihydrofuran-2-one. [HTML] [PDF]
Clive DL. Synthesis of (S)-3,4-Dihydroxybutanoic Acid Lithium Salt. [HTML] [PDF]
Clive DL. Synthesis of (R)-6-Hepten-2-ol. [HTML] [PDF]
Clive DL. Synthesis of (R)-(1-Methylhex-5-enyloxymethyl)benzene. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-(Benzyloxy)hexanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-Hydroxyhexanoic Acid. [HTML] [PDF]
Clive DL. Synthesis of (R)-5-Hydroxyhexanoic Acid Lithium Salt. [HTML] [PDF]
Clive DL. Synthesis of D-(+)-1,2:5,6-Di-O-isopropylidenemannitol. [HTML] [PDF]
Clive DL. Synthesis of (R)-2,2-Dimethyl[1,3]dioxolane-4-carbaldehyde. [HTML] [PDF]
