Triphenylarsine-catalyzed cyclopropanation: Highly stereoselective synthesis of trans-2,3-dihydro-spiro[cyclopropane-1,2′-indan-1′, 3′-dione] from alkene and phenacyl bromide

Synthetic Communications

Volumn 38, Issue 13, 2008, Pages 2200-2214

  Ren, Zhongjiao ^a   Cao, Weiguo ^a,b   Tong, Weiqi ^a   Chen, Jie ^a   Deng, Hongmei ^a   Wu, Danyi ^a  

^a SHANGHAI UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Cyclopropanation; Spirocyclopropyl compound; Stereoselective synthesis; Triphenylarsine catalyzed; Water

Indexed keywords

2,3 DIHYDRO SPIRO[CYCLOPROPANE 1,2' INDAN 1',3' DIONE]; ACETONITRILE; ALKENE; ARSINE DERIVATIVE; BENZENE; BROMIDE; CHLOROFORM; CYCLOPROPANE DERIVATIVE; DIOXANE; ORGANIC SOLVENT; SPIRO COMPOUND; SURFACTANT; TETRAHYDROFURAN; WATER;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLOPROPANATION; ISOMER; MASS SPECTROMETER; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 46749152181     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802029406     Document Type: Article

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