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

Issued Date

2005-11-03

Resource Type

Article

ISSN

00397881

DOI

10.1055/s-2005-872176

Other identifier(s)

2-s2.0-27944482117

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Synthesis. No.17 (2005), 2934-2938

Suggested Citation

Poolsak Sahakitpichan, Nopporn Thasana, Somsak Ruchirawat Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling. Synthesis. No.17 (2005), 2934-2938. doi:10.1055/s-2005-872176 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/16411

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Title

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

Author(s)

Poolsak Sahakitpichan
 Nopporn Thasana
 Somsak Ruchirawat

Other Contributor(s)

Chulabhorn Research Institute
 The Institute of Science and Technology for Research and Development, Mahidol University

Abstract

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.

Keyword(s)

Chemical Engineering
 Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/16411

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Scopus 2001-2005