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...

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Published in:Malaysian Journal of Chemistry
Main Author: Sharoman N.S.; Imran S.; Ali M.T.M.
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
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