Stoichiometry-controlled cycloaddition of azomethine ylide with dipolarophiles: Chemoselective and regioselective synthesis of bis- and tris-spirooxindole derivatives

Tetrahedron Letters

Volumn 55, Issue 16, 2014, Pages 2585-2588

  Lanka, Srinu ^a   Thennarasu, Sathiah ^a   Perumal, Paramasivan T ^a  

^a CENTRAL LEATHER RESEARCH INSTITUTE   (India)

Author keywords

Chemoselectivity; Dipolar cycloaddition; Regioselectivity; Spiro pyrrolidin 3,2 oxindole ; Spiro pyrrolidin 3,3 oxindole

Indexed keywords

AZOMETHINE YLIDE; BIS SPIROOXINDOLE DERIVATIVE; EXOCYCLIC DOUBLE BOND; OXINDOLE; TRIS SPIROOXINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLOADDITION; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STOICHIOMETRY; X RAY ANALYSIS;

EID: 84898037408     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.02.121     Document Type: Review

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