Total sytnhesis of Rhoiptelol B

Nobuhiro Tanaka; Hiroyoshi Takamura; Isao Kadota

doi:10.3987/COM-18-S(T)57

Total sytnhesis of Rhoiptelol B

Nobuhiro Tanaka, Hiroyoshi Takamura, Isao Kadota

Research output: Contribution to journal › Article › peer-review

Abstract

– A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.

Original language	English
Pages (from-to)	1157-1164
Number of pages	8
Journal	Heterocycles
Volume	97
Issue number	2
DOIs	https://doi.org/10.3987/COM-18-S(T)57
Publication status	Published - Jan 1 2018

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "Total sytnhesis of Rhoiptelol B",

abstract = "– A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.",

author = "Nobuhiro Tanaka and Hiroyoshi Takamura and Isao Kadota",

year = "2018",

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doi = "10.3987/COM-18-S(T)57",

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AU - Tanaka, Nobuhiro

AU - Takamura, Hiroyoshi

AU - Kadota, Isao

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AB - – A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.

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