N-O tethered carbenoid cyclopropanation facilitates the synthesis of a functionalized cyclopropyl-fused pyrrolidine

Journal of Organic Chemistry

Volumn 78, Issue 12, 2013, Pages 6131-6142

  Kalia, Dimpy ^a   Merey, Gökce ^a,b   Guo, Min ^a   Sintim, Herman O ^a  

^a University of Maryland   (United States)

^b HITIT UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANATION; FUNCTIONALIZED; HETEROCYCLES; INTRAMOLECULAR CYCLOPROPANATIONS; MITSUNOBU REACTIONS; PYRROLIDINE RINGS; PYRROLIDINES; STEREOGENIC CENTERS;

REACTION INTERMEDIATES; SYNTHESIS (CHEMICAL);

ORGANIC COMPOUNDS;

ALCOHOL DERIVATIVE; AMIDE; CARBENOID; CYCLOPROPANE DERIVATIVE; NITROGEN; OXYGEN; PYRROLIDINE DERIVATIVE;

ARTICLE; CHEMICAL BOND; CHEMICAL PROCEDURES; CHEMICAL STRUCTURE; CYCLOPROPANATION; MITSUNOBU REACTION; REACTION ANALYSIS; REPRODUCIBILITY; STEREOCHEMISTRY; SYNTHESIS;

ALCOHOLS; AMIDES; CATALYSIS; CYCLIZATION; CYCLOPROPANES; MOLECULAR STRUCTURE; PYRROLIDINES; STEREOISOMERISM;

EID: 84879334245     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400788a     Document Type: Article

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