Journal
TETRAHEDRON
Volume 67, Issue 9, Pages 1673-1680Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.12.068
Keywords
Asymmetric synthesis; Natural product; Amino acid; Aldol reaction; Oxazolidine
Categories
Funding
- Chinese Academy of Sciences
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Aldol reaction of 2,5-disubstituted pyrrolidine 3b with (R)-Garner aldehyde followed by Sharpless asymmetric dihydroxylation and other four reactions afforded mesylate 8a, which was introduced by an amide group via three ordinary transformations to provide amide 9a. Careful deprotection with AlCl3/Me2S and subsequent HPLC purification furnished kaitocephalin. (C) 2011 Elsevier Ltd. All rights reserved.
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