A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions

A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions

(±)-Lupinine and (±)-epilupinine have been prepared starting from commercially available δ-valerolactam. The synthetic route involves the advantages of the cyclization based on α-sulfmyl carbanions.

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Main Authors: Manat Pohmakotr, Anusorn Seubsai, Pornthep Numeechai, Patoomratana Tuchinda
Other Authors: Mahidol University
Format: Article
Published: 2018
Subjects:
Chemical Engineering
Chemistry
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/19041
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Institution: Mahidol University
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spelling th-mahidol.190412018-07-12T09:22:52Z A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions Manat Pohmakotr Anusorn Seubsai Pornthep Numeechai Patoomratana Tuchinda Mahidol University Chemical Engineering Chemistry (±)-Lupinine and (±)-epilupinine have been prepared starting from commercially available δ-valerolactam. The synthetic route involves the advantages of the cyclization based on α-sulfmyl carbanions. 2018-07-12T02:21:24Z 2018-07-12T02:21:24Z 2008-06-02 Article Synthesis. No.11 (2008), 1733-1736 10.1055/s-2008-1067027 00397881 2-s2.0-45249124488 https://repository.li.mahidol.ac.th/handle/123456789/19041 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=45249124488&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Chemical Engineering
Chemistry
spellingShingle Chemical Engineering
Chemistry
Manat Pohmakotr
Anusorn Seubsai
Pornthep Numeechai
Patoomratana Tuchinda
A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
description (±)-Lupinine and (±)-epilupinine have been prepared starting from commercially available δ-valerolactam. The synthetic route involves the advantages of the cyclization based on α-sulfmyl carbanions.
author2 Mahidol University
author_facet Mahidol University
Manat Pohmakotr
Anusorn Seubsai
Pornthep Numeechai
Patoomratana Tuchinda
format Article
author Manat Pohmakotr
Anusorn Seubsai
Pornthep Numeechai
Patoomratana Tuchinda
author_sort Manat Pohmakotr
title A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
title_short A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
title_full A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
title_fullStr A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
title_full_unstemmed A new strategy for the synthesis of (±)-Lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
title_sort new strategy for the synthesis of (±)-lupinine and (±)-epilupinine via cyclization of α-sulfinyl carbanions
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/19041
_version_ 1763496397131218944

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