A highly regioselective synthesis of 1-N-methyl-spiro-[2,3‴1]- oxindole-spiro-[3,2″]indane-1″, 3″-dione-4-arylpyrrolidines through 1,3-dipolar cycloaddition protocol

Journal of Heterocyclic Chemistry

Volumn 43, Issue 6, 2006, Pages 1467-1472

  Babu, A R Suresh ^a   Raghunathan, R ^a   Gayatri, G ^b   Sastry, G Narahari ^b  

^a UNIVERSITY OF MADRAS   (India)

^b INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AZOMETHINE YLIDE; ISATIN; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRROLIDINE DERIVATIVE; SARCOSINE;

ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLOADDITION; DECARBOXYLATION; DENSITY FUNCTIONAL THEORY; ENERGY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 33845447165     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570430609     Document Type: Article

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