Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82679
Title: A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
Authors: Ding, Feiqing
William, Ronny
Kock, Si Min
Leow, Min Li
Liu, Xue-Wei
Keywords: azetidine
glycosylation
Issue Date: 2015
Source: Ding, F., William, R., Kock, S. M., Leow, M. L., & Liu, X.-W. (2015). A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B. Chemical Communications, 51(22), 4639-4642.
Series/Report no.: Chemical Communications
Abstract: An efficient and high-yielding synthesis of penaresidin B is disclosed herein. The concise 8-step synthesis of azetidine aldehyde was devised by incorporating our novel strategy for ready access to 3-amino-2,3-dideoxysugars via regio- and stereoselective tandem hydroamination/glycosylation of glycal as the key step.
URI: https://hdl.handle.net/10356/82679
http://hdl.handle.net/10220/40279
ISSN: 1359-7345
DOI: 10.1039/C4CC09904D
Schools: School of Physical and Mathematical Sciences 
Rights: This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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