Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes
A new asymmetric synthesis of several hydroxy N,O-heterobicyclic octanes is described in this paper. The synthesis employed Salen catalysed epoxide ring opening of the starting material meso-cyclohexene followed by the azide reduction and NBoc protection of (1S,6S)-6-azido-3-cyclohexenol, allylic hy...
Published in: | Malaysian Journal of Chemistry |
---|---|
Main Author: | |
Format: | Conference paper |
Language: | English |
Published: |
Malaysian Institute of Chemistry
2022
|
Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133513339&partnerID=40&md5=a1bf76ed85bd8ee08de14a84a9df42c3 |
id |
2-s2.0-85133513339 |
---|---|
spelling |
2-s2.0-85133513339 Sharoman N.S.; Imran S.; Ali M.T.M. Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes 2022 Malaysian Journal of Chemistry 24 2 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133513339&partnerID=40&md5=a1bf76ed85bd8ee08de14a84a9df42c3 A new asymmetric synthesis of several hydroxy N,O-heterobicyclic octanes is described in this paper. The synthesis employed Salen catalysed epoxide ring opening of the starting material meso-cyclohexene followed by the azide reduction and NBoc protection of (1S,6S)-6-azido-3-cyclohexenol, allylic hydroxylation and lactonization with final carbonyl reduction to produce hydroxy N,O-heterobicyclic octane. © 2022 Malaysian Institute of Chemistry. All rights reserved. Malaysian Institute of Chemistry 15112292 English Conference paper |
author |
Sharoman N.S.; Imran S.; Ali M.T.M. |
spellingShingle |
Sharoman N.S.; Imran S.; Ali M.T.M. Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
author_facet |
Sharoman N.S.; Imran S.; Ali M.T.M. |
author_sort |
Sharoman N.S.; Imran S.; Ali M.T.M. |
title |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
title_short |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
title_full |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
title_fullStr |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
title_full_unstemmed |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
title_sort |
Asymmetric Synthesis of Hydroxy N,O-Heterobicyclic Octanes |
publishDate |
2022 |
container_title |
Malaysian Journal of Chemistry |
container_volume |
24 |
container_issue |
2 |
doi_str_mv |
|
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133513339&partnerID=40&md5=a1bf76ed85bd8ee08de14a84a9df42c3 |
description |
A new asymmetric synthesis of several hydroxy N,O-heterobicyclic octanes is described in this paper. The synthesis employed Salen catalysed epoxide ring opening of the starting material meso-cyclohexene followed by the azide reduction and NBoc protection of (1S,6S)-6-azido-3-cyclohexenol, allylic hydroxylation and lactonization with final carbonyl reduction to produce hydroxy N,O-heterobicyclic octane. © 2022 Malaysian Institute of Chemistry. All rights reserved. |
publisher |
Malaysian Institute of Chemistry |
issn |
15112292 |
language |
English |
format |
Conference paper |
accesstype |
|
record_format |
scopus |
collection |
Scopus |
_version_ |
1809677892810964992 |