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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/16411
Title: Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling
Authors: Poolsak Sahakitpichan
Nopporn Thasana
Somsak Ruchirawat
Chulabhorn Research Institute
The Institute of Science and Technology for Research and Development, Mahidol University
Keywords: Chemical Engineering;Chemistry
Issue Date: 3-Nov-2005
Citation: Synthesis. No.17 (2005), 2934-2938
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27944482117&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/16411
ISSN: 00397881
Appears in Collections:Scopus 2001-2005

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