Nitrile and amide biotransformations for the synthesis of enantiomerically pure 3-arylaziridine-2-carboxamide derivatives and their stereospecific ring-opening reactions

Journal of Organic Chemistry

Volumn 72, Issue 24, 2007, Pages 9391-9394

  Wang, Jin Yuan ^a   Wang, De Xian ^a   Pan, Jie ^a   Huang, Zhi Tang ^a   Wang, Mei Xiang ^a  

^a INSTITUTE OF CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE BIOTRANSFORMATIONS; NITRILE HYDRATASE; RING-OPENING REACTIONS;

AMIDES; AMINES; CATALYST ACTIVITY; ENANTIOMERS; HYDROGENATION; SYNTHESIS (CHEMICAL);

DERIVATIVES;

AMIDE; AMINE; AZIRIDINE 2 CARBOXAMIDE DERIVATIVE; AZIRIDINE DERIVATIVE; NITRILE; NITRILE HYDRATASE; PROPIONAMIDE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL MODIFICATION; ENANTIOMER; HYDROGENATION; NONHUMAN; REACTION ANALYSIS; RHODOCOCCUS ERYTHROPOLIS; RING OPENING; STEREOSPECIFICITY; SYNTHESIS;

AMIDES; AMINES; AZIRIDINES; BIOTRANSFORMATION; CATALYSIS; HYDRO-LYASES; HYDROGENATION; MODELS, CHEMICAL; NITRILES; RHODOCOCCUS; STEREOISOMERISM; TRIFLUOROACETIC ACID; WATER;

EID: 36649017440     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701732h     Document Type: Article

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