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|Title:||Efficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-coupling|
Chulabhorn Research Institute
The Institute of Science and Technology for Research and Development, Mahidol University
|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.|
|Appears in Collections:||Scopus 2001-2005|
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