Regioselective and stereoselective nucleophilic ring opening of trifluoromethylated cyclic sulfates: Asymmetric synthesis of both enantiomers of syn-(3-trifluoromethyl)isoserine

Journal of Organic Chemistry

Volumn 69, Issue 16, 2004, Pages 5486-5489

  Jiang, Zhong Xing ^a   Qing, Feng Ling ^a,b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b DONGHUA UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGENATION; OXIDATION; SYNTHESIS (CHEMICAL);

ENANTIOMERS; STEREOSELECTIVE NUCLEOPHILICITY;

AROMATIC COMPOUNDS;

(3 TRIFLUOROMETHYL)ISOSERINE; (N BENZOYL) 3 (TRIFLUOROMETHYL)ISOSERINE; BETA AMINO ACID; DISULFIDE; FLUORINE DERIVATIVE; ISOSERINE; METHYL GROUP; SODIUM AZIDE; SULFATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOMER; HYDROGENOLYSIS; JONES OXIDATION; REACTION ANALYSIS; RING OPENING; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

CATALYSIS; CYCLIZATION; HYDROCARBONS, FLUORINATED; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; SERINE; STEREOISOMERISM; SULFATES;

EID: 3543029840     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0497611     Document Type: Article

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