Stereoselective synthesis of unsaturated and functionalized L-NHBoc amino acids, using wittig reaction under mild phase-transfer conditions

Journal of Organic Chemistry

Volumn 77, Issue 17, 2012, Pages 7579-7587

  Rémond, Emmanuelle ^a   Bayardon, Jérôme ^a   Ondel Eymin, Marie Joëlle ^a   Jugé, Sylvain ^a  

^a UNIVERSITÉ DE BOURGOGNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALIPHATIC ALDEHYDES; CARBOXYLIC ACID GROUPS; DEPROTECTION; FERROCENYL; FUNCTIONALIZED; L-ASPARTIC ACID; LATERAL CHAINS; PALLADIUM-CATALYZED; PHASE-TRANSFER CONDITIONS; PHOSPHONIUM SALTS; QUATERNIZATION; SOLID-LIQUID; STEREOSELECTIVE SYNTHESIS; TRIFLUOROACETOPHENONE; TRIFLUOROMETHYL; TRIPHENYL PHOSPHINES; UNSATURATED ALDEHYDES; UNSATURATED AMINO ACIDS; WEAK BASE; WITTIG REACTION; WITTIG REAGENTS;

ALDEHYDES; CARBOXYLIC ACIDS; CHEMICAL REACTIONS; OLEFINS; ORGANIC COMPOUNDS; STEREOCHEMISTRY; STEREOSELECTIVITY;

AMINO ACIDS;

ALDEHYDE; ALLYL 4 IODOBUTANOATE; ALPHA AMINO ACID; ASPARTIC ACID; AZIDE; CARBOXYLIC ACID; CHLOROBENZENE; FERROCENE DERIVATIVE; FUNCTIONAL GROUP; PALLADIUM; PHOSPHONIUM DERIVATIVE; TRIPHENYLPHOSPHINE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; ENANTIOSELECTIVITY; ISOMERIZATION; MELTING POINT; PROTEIN SYNTHESIS; RACEMIZATION; STEREOCHEMISTRY; WITTIG REACTION;

AMINO ACIDS; MOLECULAR CONFORMATION; PHASE TRANSITION; STEREOISOMERISM;

EID: 84866141125     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3013622     Document Type: Article

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