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A Unifying Stereochemical Analysis for the Formation of Halogenated C-15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Epoxide

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Title: A Unifying Stereochemical Analysis for the Formation of Halogenated C-15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Epoxide
Authors: Bonney, KJ
Braddock, DC
Item Type: Journal Article
Issue Date: 2-Nov-2012
URI: http://hdl.handle.net/10044/1/15219
DOI: http://dx.doi.org/10.1021/jo301580c
ISSN: 0022-3263
Publisher: AMER CHEMICAL SOC
Start Page: 9574
End Page: 9584
Journal / Book Title: JOURNAL OF ORGANIC CHEMISTRY
Volume: 77
Issue: 21
Copyright Statement: Copyright © 2012 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo301580c
Publication Status: Published
Appears in Collections:Chemistry