A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B

A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B

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...

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Main Authors: Ding, Feiqing, William, Ronny, Kock, Si Min, Leow, Min Li, Liu, Xue-Wei
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2016
Subjects:
azetidine
glycosylation
Online Access:https://hdl.handle.net/10356/82679
http://hdl.handle.net/10220/40279
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-82679
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spelling sg-ntu-dr.10356-826792023-02-28T19:29:07Z A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B Ding, Feiqing William, Ronny Kock, Si Min Leow, Min Li Liu, Xue-Wei School of Physical and Mathematical Sciences azetidine glycosylation 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. MOE (Min. of Education, S’pore) Published version 2016-03-15T06:26:46Z 2019-12-06T15:00:14Z 2016-03-15T06:26:46Z 2019-12-06T15:00:14Z 2015 Journal Article 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. 1359-7345 https://hdl.handle.net/10356/82679 http://hdl.handle.net/10220/40279 10.1039/C4CC09904D en Chemical Communications This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. 4 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic azetidine
glycosylation
spellingShingle azetidine
glycosylation
Ding, Feiqing
William, Ronny
Kock, Si Min
Leow, Min Li
Liu, Xue-Wei
A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
description 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.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Ding, Feiqing
William, Ronny
Kock, Si Min
Leow, Min Li
Liu, Xue-Wei
format Article
author Ding, Feiqing
William, Ronny
Kock, Si Min
Leow, Min Li
Liu, Xue-Wei
author_sort Ding, Feiqing
title A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
title_short A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
title_full A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
title_fullStr A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
title_full_unstemmed A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B
title_sort concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin b
publishDate 2016
url https://hdl.handle.net/10356/82679
http://hdl.handle.net/10220/40279
_version_ 1759856200545992704

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