Stereoselective synthesis of highly functionalized nitrocyclopropanes through the organocatalyic Michael-addition-initiated cyclization of bromonitromethane and β,γ-unsaturated α-ketoesters

Chemistry - An Asian Journal

Volumn 8, Issue 11, 2013, Pages 2859-2863

  Yu, Haijian ^a   Wang, Qiaohui ^a   Wang, Youming ^a   Song, Haibing ^a   Zhou, Zhenghong ^a   Tang, Chuchi ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

alkylation; asymmetric catalysis; Michael addition; nitrocyclopropanes; organocatalysis

Indexed keywords

ASYMMETRIC CATALYSIS; CYCLOPROPANATION; ENANTIOSELECTIVE; MICHAEL ADDITIONS; NITROCYCLOPROPANES; ORGANOCATALYSIS; STEREOCONTROLLED SYNTHESIS; STEREOSELECTIVE SYNTHESIS;

ADDITION REACTIONS; ALKYLATION; ENANTIOSELECTIVITY; REACTION KINETICS; STEREOCHEMISTRY; STEREOSELECTIVITY;

CATALYSIS;

BROMONITROMETHANE; CYCLOPROPANE DERIVATIVE; DRUG DERIVATIVE; ESTER; ETHANE; NITRO DERIVATIVE;

ALKYLATION; ARTICLE; ASYMMETRIC CATALYSIS; CATALYSIS; CHEMISTRY; CONFORMATION; CYCLIZATION; MICHAEL ADDITION; NITROCYCLOPROPANES; ORGANOCATALYSIS; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ALKYLATION; ASYMMETRIC CATALYSIS; MICHAEL ADDITION; NITROCYCLOPROPANES; ORGANOCATALYSIS;

ALKYLATION; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; CYCLOPROPANES; ESTERS; ETHANE; MOLECULAR CONFORMATION; NITRO COMPOUNDS; STEREOISOMERISM;

EID: 84887019078     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201300778     Document Type: Article

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