Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone

On treatment with acids, the open-chained amide acetals (1) gave the 7,7 membered ring fused benzazepinones (4) via the bis-cyclisation. © 2008 The Japan Institute of Heterocyclic Chemistry.

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Main Authors: Wong Phakhodee, Poolsak Sahakitpichan, Songpon Deechongkit, Somsak Ruchirawat
Other Authors: Chulabhorn Research Institute
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/19074
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spelling th-mahidol.190742018-07-12T09:50:28Z Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone Wong Phakhodee Poolsak Sahakitpichan Songpon Deechongkit Somsak Ruchirawat Chulabhorn Research Institute Chulabhorn Graduate Institute Mahidol University The Institute of Science and Technology for Research and Development, Mahidol University Chemistry Pharmacology, Toxicology and Pharmaceutics On treatment with acids, the open-chained amide acetals (1) gave the 7,7 membered ring fused benzazepinones (4) via the bis-cyclisation. © 2008 The Japan Institute of Heterocyclic Chemistry. 2018-07-12T02:22:33Z 2018-07-12T02:22:33Z 2008-08-01 Article Heterocycles. Vol.75, No.8 (2008), 1963-1970 10.3987/COM-08-11366 03855414 2-s2.0-54249159680 https://repository.li.mahidol.ac.th/handle/123456789/19074 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=54249159680&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 Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Chemistry
Pharmacology, Toxicology and Pharmaceutics
Wong Phakhodee
Poolsak Sahakitpichan
Songpon Deechongkit
Somsak Ruchirawat
Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
description On treatment with acids, the open-chained amide acetals (1) gave the 7,7 membered ring fused benzazepinones (4) via the bis-cyclisation. © 2008 The Japan Institute of Heterocyclic Chemistry.
author2 Chulabhorn Research Institute
author_facet Chulabhorn Research Institute
Wong Phakhodee
Poolsak Sahakitpichan
Songpon Deechongkit
Somsak Ruchirawat
format Article
author Wong Phakhodee
Poolsak Sahakitpichan
Songpon Deechongkit
Somsak Ruchirawat
author_sort Wong Phakhodee
title Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
title_short Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
title_full Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
title_fullStr Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
title_full_unstemmed Investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
title_sort investigation of the acid-mediated cyclisation of amide acetal for the synthesis of benzazepinone
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/19074
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