Stereoselective construction of 2-vinyl 3-hydroxybenzopyran rings: total syntheses of teadenols A and B-Reference-Cited by-同舟云学术

Stereoselective construction of 2-vinyl 3-hydroxybenzopyran rings: total syntheses of teadenols A and B

Published:2016 Issue:46 Volume:14 Page:10783-10786
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yoshida Ryunosuke¹²³⁴,Ouchi Hitoshi¹²³⁴,Yoshida Atsushi¹²³⁴,Asakawa Tomohiro¹²³⁴,Inai Makoto¹²³⁴,Egi Masahiro¹²³⁴,Hamashima Yoshitaka¹²³⁴,Kan Toshiyuki¹²³⁴

Affiliation:

1. School of Pharmaceutical Sciences

2. University of Shizuoka

3. Shizuoka 422-8526

4. Japan

Abstract

Total syntheses of teadenols A and B, isolated from fermented tea, were accomplished in a highly stereocontrolled manner.

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB02004F

Reference22 articles.

1. New phenolic compounds from Camellia sinensis L. leaves fermented with Aspergillus sp.

2. Synthetic Studies of Fisetin, Myricetin and Nobiletin Analogs and Related Probe Molecules

3. Enantioselective Total Synthesis of Aperidine

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