ChemInform Abstract: SUBSTITUENT, REAGENT, AND SOLVENT EFFECTS ON THE STERIC COURSE OF ADDITIONS INITIATED BY ELECTROPHILIC BROMINE TO 3‐BROMOCYCLOHEXENE. COMPARISON WITH THE STEREOSELECTIVITY OF EPOXIDATION AND THE REGIOSELECTIVITY OF RING OPENING OF EPOXIDES

Abstract

Chemischer InformationsdienstVolume 7, Issue 7 Preparative Organic Chemistry ChemInform Abstract: SUBSTITUENT, REAGENT, AND SOLVENT EFFECTS ON THE STERIC COURSE OF ADDITIONS INITIATED BY ELECTROPHILIC BROMINE TO 3-BROMOCYCLOHEXENE. COMPARISON WITH THE STEREOSELECTIVITY OF EPOXIDATION AND THE REGIOSELECTIVITY OF RING OPENING OF EPOXIDES P. L. BARILI, P. L. BARILISearch for more papers by this authorG. BELLUCCI, G. BELLUCCISearch for more papers by this authorF. MARIONI, F. MARIONISearch for more papers by this authorV. SCARTONI, V. SCARTONISearch for more papers by this author P. L. BARILI, P. L. BARILISearch for more papers by this authorG. BELLUCCI, G. BELLUCCISearch for more papers by this authorF. MARIONI, F. MARIONISearch for more papers by this authorV. SCARTONI, V. SCARTONISearch for more papers by this author First published: February 17, 1976 https://doi.org/10.1002/chin.197607139Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume7, Issue7February 17, 1976 RelatedInformation