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Masato Nozawa

4 papers in the library · 65 citations · publishing 2008-2010

Papers

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ChemInform Abstract: Highly Oxygenated Diterpenoids Associated to the Central Nervous System: Syntheses of Salvinorin and Forskolin

ChemInform May 4, 2010 Hisahiro Hagiwara, Masato Nozawa

Abstract: ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Highly Oxygenated Diterpenoids Associated to the Central Nervous System: Syntheses of Salvinorin and Forskolin

Journal of Synthetic Organic Chemistry Japan 2009 Hisahiro Hagiwara, Masato Nozawa 2 citations

Total synthesis of salvinorin A (1), a densely functionalized neoclerodane diterpenoid, having the most potent hallucinogenic activity and a selective κ–opioid agonist, has been completed in 20 steps starting from enantiomerically–pure Wieland–Miescher ketone derivative 23. Subsequently, alternative total synthesis of salvinorin A (1) has been developed via palladium–catalyzed double...

ChemInform Abstract: Total Synthesis of the Hallucinogenic Neoclerodane Diterpenoid Salvinorin A.

ChemInform August 26, 2008 Masato Nozawa, Yuhki Suka, Takashi Hoshi et al.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Total synthesis of the hallucinogenic neoclerodane diterpenoid salvinorin A.

Organic Letters April 3, 2008 Masato Nozawa, Yuhki Suka, Takashi Hoshi et al. 63 citations

Total synthesis of salvinorin A (1), a neoclerodane diterpenoid having the most potent hallucinogenic activity and a selective kappa-opioid agonist, was completed in 20 steps starting from enantiomerically pure hydroxy-Wieland-Miescher ketone 5.