Reductive S <sub>N</sub> 2’ Reaction of Epoxydienoate with Borane and its Application to the Synthesis and Structural Revision of an Antitumor Active Torrubiellutin Analogue-Reference-Cited by-同舟云学术

Reductive S _N 2’ Reaction of Epoxydienoate with Borane and its Application to the Synthesis and Structural Revision of an Antitumor Active Torrubiellutin Analogue

Published:2022-08-18 Issue:18 Volume:17 Page:
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chemistry An Asian Journal

Author:

Murokawa Shunsuke¹,Furukawa Koki¹,Kawano Yoshinori¹,Nihei Tsukasa¹,Suzuki Yuji²,Yasui Eiko¹,Nagumo Shinji¹^ORCID

Affiliation:

1. Department of Chemistry and Life Science Kogakuin University Nakano 2665-1 192-0015 Hachioji Tokyo Japan

2. Department of Medicinal Chemistry Faculty of Pharmaceutical Sciences Hokkaido University of Science Maeda 7-15-4-1, Teine 006-8585 Sapporo Hokkaido Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.202200650

Reference48 articles.

1. Stereospecific methylation of .gamma.,.delta.-epoxy acrylates by trimethylaluminum: a method for the iterative construction of polypropionate chains

2. Palladium-catalyzed selective hydrogenolysis of alkenyloxiranes with formic acid. Stereoselectivity and synthetic utility

3. A regio- and stereoselective α-methylation of γ,δ-epoxy-α,β-unsaturated esters with a Me2Zn–CuCN reagent

5. Isolierung von Venturicidin X, dem Aglycon der Venturicidine A und B aus Streptomyceten / Isolation of Venturicidin X, the Aglycon of Venturicidines A and B from Streptopyces sp

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