Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2-Position Using 8-Phenylmenthol as the Chiral Auxiliary-Reference-Cited by-同舟云学术

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Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2-Position Using 8-Phenylmenthol as the Chiral Auxiliary

Published:2014-06-05 Issue:6 Volume:43 Page:766-768
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Katori Aki¹,Sashihara Yoshiaki¹,Iwamoto Akihisa¹,Kojima Satoshi¹²,Yamamoto Yohsuke¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Hiroshima University

2. Center for Quantum Life Sciences, Hiroshima University

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/cl.140052

Reference35 articles.

1. Five-membered heteroaromatic rings as intermediates in organic synthesis

2. Synthetic applications of furan Diels-Alder chemistry

3. The use of furans in natural product syntheses

4. Use of furans in synthesis of bioactive compounds

5. Regiospecific synthesis of polysubstituted furans and their application in organic synthesis

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ChemInform Abstract: Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2-Position Using 8-Phenylmenthol as the Chiral Auxiliary.;ChemInform;2014-10-02

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