Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/75946
Title: An approach to the welwistatin core via a diazoketone rearrangement-ring expansion strategy
Authors: Lam, SM
Wong, WT 
Chiu, P
Issue Date: 2017
Publisher: American Chemical Society
Source: Organic letters, 2017, v. 19, no. 17, p. 4468-4471 How to cite?
Journal: Organic letters 
Abstract: The rhodium-catalyzed decomposition of fused bicyclic alpha-diazo-beta-hydroxyketone 16 and rearrangement to 17 is featured in an approach to the bridged bicyclic core of welwistatin. The bicyclic [4.3.1] core of 25 is furnished from a subsequent cyclopropanation to generate 23, followed by its ring expansion.
URI: http://hdl.handle.net/10397/75946
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/acs.orglett.7b01988
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