Poolsak SahakitpichanNopporn ThasanaSomsak RuchirawatChulabhorn Research InstituteThe Institute of Science and Technology for Research and Development, Mahidol University2018-06-212018-06-212005-11-03Synthesis. No.17 (2005), 2934-2938003978812-s2.0-27944482117https://repository.li.mahidol.ac.th/handle/20.500.14594/16411Tetramethoxydiospyrol 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.Mahidol UniversityChemical EngineeringChemistryEfficient synthesis of diospyrol via Suzuki-Miyaura and modified in situ cross-couplingArticleSCOPUS10.1055/s-2005-872176