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...
Saved in:
| Main Authors: | , , , , |
|---|---|
| 其他作者: | |
| 格式: | Article |
| 語言: | English |
| 出版: |
2016
|
| 主題: | |
| 在線閱讀: | https://hdl.handle.net/10356/82679 http://hdl.handle.net/10220/40279 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
| 機構: | Nanyang Technological University |
| 語言: | English |
| id |
sg-ntu-dr.10356-82679 |
|---|---|
| record_format |
dspace |
| 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 |