Enantioselective [4+2] cycloadditions of 2-vinyl-1 H-indoles with 3-nitro-2 H-chromenes catalyzed by a Zn(OTf) 2/bis(oxazoline) complex: An efficient approach to fused heterocycles with a quaternary stereocenter

Chemistry - An Asian Journal

Volumn 7, Issue 3, 2012, Pages 493-497

  Tan, Fen ^a   Xiao, Cong ^b   Cheng, Hong Gang ^a   Wu, Wei ^a   Ding, Ke Rong ^a   Xiao, Wen Jing ^a  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

^b PEKING UNIVERSITY   (China)

Author keywords

cycloaddition; enantioselectivity; heterocycles; indoles; Lewis acid catalysis

Indexed keywords

[4+2] CYCLOADDITION REACTIONS; CYCLOADDITIONS; ENANTIOSELECTIVE; HETEROCYCLES; INDOLES; LEWIS ACID CATALYSIS; OXAZOLINES; QUATERNARY STEREOCENTERS; REACTION EFFICIENCY;

CATALYSIS; CYCLOADDITION; NITROGEN COMPOUNDS; ZINC;

ENANTIOSELECTIVITY;

BENZOPYRAN DERIVATIVE; HETEROCYCLIC COMPOUND; INDOLE DERIVATIVE; MESYLIC ACID DERIVATIVE; OXAZOLE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

BENZOPYRANS; CYCLIZATION; HETEROCYCLIC COMPOUNDS; INDOLES; MESYLATES; MOLECULAR STRUCTURE; OXAZOLES; STEREOISOMERISM;

EID: 84857752743     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201100820     Document Type: Article

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