Synthesis of spiropyrrolidines and spiropyrrolizidines by azomethine ylide cycloaddition of baylis-hillman adducts derived from N -methyl maleimide

Synlett

Volumn , Issue 18, 2010, Pages 2751-2754

  Karthikeyan, K ^a   Saranya, N ^a   Kalaivani, A ^a   Perumal, P T ^a  

^a CENTRAL LEATHER RESEARCH INSTITUTE   (India)

Author keywords

azomethine ylide cycloadditon; Baylis Hillman reaction; spiropyrrolidines; spiropyrrolizidines

Indexed keywords

3A' (3 HYDROXY 1 METHYL 2 OXOINDOLIN 3 YL) 1,2',5' TRIMETHYL 3',3A' DIHYDRO 2' H SPIRO[INDOLINE 3,1' PYRROLO[3,4 C]PYRROLE] 2,4',6' (5'H,6A'H) TRIONE; 8B' (1 ETHYL 3 HYDROXY 2 OXOINDOLIN 3 YL) 1,2' DIMETHYL 6',7',8',8A' TETRAHYDRO 1'H SPIRO[INDOLINE 3,4' PYRROLO[3,4 A]PYRROLIZINE] 1',2,3' (2'H,3A'H,8B'H) TRIONE; ALSTONISINE; AZOMETHINE YLIDE; ELACOMINE; HORSFILINE; ISATIN DERIVATIVE; MALEIMIDE DERIVATIVE; N METHYLMALEIMIDE; PYRROLIDINE DERIVATIVE; SARCOSINE; SPIROPYRROLIDINE DERIVATIVE; SPIROPYRROLIZIDINE DERIVATIVE; SPIROTRYPROSTATIN A; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; CRYSTAL STRUCTURE; CYCLOADDITION; DECARBOXYLATION; DRUG STRUCTURE; DRUG SYNTHESIS; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 78149284378     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1258810     Document Type: Article

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