An unprecedented chemospecific and stereoselective tandem nucleophilic addition/cycloaddition reaction of Nucleophilic carbenes with ketenimines

Journal of Organic Chemistry

Volumn 74, Issue 2, 2009, Pages 850-855

  Cheng, Ying ^a   Yang Guang, Ma ^a   Wang, Xiao Rong ^a   Mo, Jun Ming ^a  

^a BEIJING NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOTHIAZOLE; C-C BONDS; CARBENE; CARBENES; DIPOLAR INTERMEDIATES; GOOD YIELDS; KETENIMINE; KETENIMINES; NUCLEOPHILIC ADDITIONS; PYRROLE DERIVATIVES; STEREO-SELECTIVE; STEREOSELECTIVE MANNERS;

NITROGEN COMPOUNDS;

1,3 DIPOLAR; AMPHOLYTE; BENZOTHIAZOLE; BENZOTHIAZOLE SPIROPYRROLE; CARBENOID; CARBON; IMINE; KETENIMINE; NITROGEN; NUCLEOPHILE; PYRROLE DERIVATIVE; SPIRO COMPOUND; THIAZOLE; THIAZOLE SPIROPYRROLE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL INTERACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHEMOSENSITIZATION; CYCLIZATION; CYCLOADDITION; ENERGY YIELD; STEREOCHEMISTRY; TANDEM MASS SPECTROMETRY;

EID: 64549159403     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802289s     Document Type: Article

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