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Volumn 58, Issue 17, 2002, Pages 3371-3378

Diastereoselectivity of tandem Michael addition-alkylation reactions: A convenient method for one-pot synthesis of α-branched 2,3-diphenylglutaric acid derivatives

(5) Viteva, L a Gospodova, Tz a Stefanovsky, Y a Angelova, S a Gorrichon, L b

a INSTITUTE OF ORGANIC CHEMISTRY (Bulgaria)

b Université Paul Sabatier Toulouse III (France)

Author keywords

Alkylations; Asymmetric induction; Diastereoselectivity; Michael additions; Tandem reactions

Indexed keywords

2,3 DIPHENYL 2 METHYLPENTADIOIC ACID 1,5 BIS(DIMETHYLAMIDE); 4 CYANO 3,4 DIPHENYLPENTANOIC ACID DIMETHYLAMIDE; 4 CYANO 3,4 DIPHENYLPENTANOIC ACID TERT BUTYL ESTER; AMIDE; ESTER DERIVATIVE; GLUTARIC ACID DERIVATIVE; NITRILE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; ASYMMETRIC SYNTHESIS; CHELATION; CHEMICAL REACTION; CHIRALITY; CYCLOADDITION; DIASTEREOISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; STEREOCHEMISTRY; TANDEM MICHAEL ADDITION; THIN LAYER CHROMATOGRAPHY;

EID: 0037156636 PISSN: 00404020 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4020(02)00298-3 Document Type: Article

Times cited : (3)

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