Stereochemistry of the [3+2] cycloaddition of acrylonitrile to the N-oxide of 5-methyl-4,5-dihydro-3H-spiro[benz-2-azepine-3,1′-cyclohexane]

Chemistry of Heterocyclic Compounds

Volumn 37, Issue 10, 2001, Pages 1244-1250

  Varlamov, A V ^a   Zubkov, F I ^a   Turchin, K F ^b   Chernyshev, A I ^a   Borisov, R S ^a  

^a PEOPLES FRIENDSHIP UNIVERSITY OF RUSSIA   (Russian Federation)

^b Center for Drug Chemistry   (Russian Federation)

Author keywords

3+2 cycloaddition; Alkenes; Benz 2 azepines; Cyclic nitrones; Spiro compounds

Indexed keywords

5 METHYL 4,5 DIHYDRO 3H SPIRO(BENZ 2 AZEPINE 3,1' CYCLOHEXANE); ACRYLONITRILE; AZEPINE DERIVATIVE; OXIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; ISOMER; KINETICS; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; THERMODYNAMICS;

EID: 0035495057     PISSN: 00093122     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1013853728211     Document Type: Article

References (13)

1. The [3+2]-nitrone olefine cycloaddition reaction