Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling

Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling

Tetramethoxydiospyrol was synthesized via Suzuki-Miyaura cross-coupling of the two key intermediates, halonaphthalene and naphthaleneboronic acid derivatives, which were derived from the same naphthol. Moreover, the product could be conveniently obtained by a one-pot modified in situ Suzuki coupling...

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Main Authors: Poolsak Sahakitpichan, Nopporn Thasana, Somsak Ruchirawat
Other Authors: Chulabhorn Research Institute
Format: Article
Published: 2018
Subjects:
Chemical Engineering
Chemistry
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/16411
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Institution: Mahidol University
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spelling th-mahidol.164112018-06-21T15:11:33Z Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling Poolsak Sahakitpichan Nopporn Thasana Somsak Ruchirawat Chulabhorn Research Institute The Institute of Science and Technology for Research and Development, Mahidol University Chemical Engineering Chemistry Tetramethoxydiospyrol was synthesized via Suzuki-Miyaura cross-coupling of the two key intermediates, halonaphthalene and naphthaleneboronic acid derivatives, which were derived from the same naphthol. Moreover, the product could be conveniently obtained by a one-pot modified in situ Suzuki coupling. The naphthol was synthesized via the cyclization of ortho-allylbenzamide intermediate. © Georg Thieme Verlag Stuttgart. 2018-06-21T08:11:16Z 2018-06-21T08:11:16Z 2005-11-03 Article Synthesis. No.17 (2005), 2934-2938 10.1055/s-2005-872176 00397881 2-s2.0-27944482117 https://repository.li.mahidol.ac.th/handle/123456789/16411 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27944482117&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
Poolsak Sahakitpichan
Nopporn Thasana
Somsak Ruchirawat
Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
description Tetramethoxydiospyrol was synthesized via Suzuki-Miyaura cross-coupling of the two key intermediates, halonaphthalene and naphthaleneboronic acid derivatives, which were derived from the same naphthol. Moreover, the product could be conveniently obtained by a one-pot modified in situ Suzuki coupling. The naphthol was synthesized via the cyclization of ortho-allylbenzamide intermediate. © Georg Thieme Verlag Stuttgart.
author2 Chulabhorn Research Institute
author_facet Chulabhorn Research Institute
Poolsak Sahakitpichan
Nopporn Thasana
Somsak Ruchirawat
format Article
author Poolsak Sahakitpichan
Nopporn Thasana
Somsak Ruchirawat
author_sort Poolsak Sahakitpichan
title Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
title_short Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
title_full Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
title_fullStr Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
title_full_unstemmed Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
title_sort efficient synthesis of diospyrol via suzuki-miyaura and modified in situ cross-coupling
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/16411
_version_ 1763497708723634176

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