Synthesis of γ- and δ-Lactone Natural Products by Employing a trans–cis Isomerization/Lactonization Strategy-Reference-Cited by-同舟云学术

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Synthesis of γ- and δ-Lactone Natural Products by Employing a trans–cis Isomerization/Lactonization Strategy

Published:2013 Issue:4 Volume:61 Page:464-470
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

Ono Machiko¹,Kato Keisuke²,Akita Hiroyuki¹

Affiliation:

1. School of Pharmaceutical Sciences, International University of Health and Welfare

2. Faculty of Pharmaceutical Sciences, Toho University

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

https://www.jstage.jst.go.jp/article/cpb/61/4/61_c12-01026/_pdf

Reference13 articles.

1. 1) Still W. C., Gennari C., Tetrahedron Lett., 24, 4405–4408 (1983).

2. 2) Chatterjee A. K., Morgan J. P., Scholl M., Grubbs R. H., J. Am. Chem. Soc., 122, 3783–3784 (2000).

3. 3) Ono M., Saotome C., Akita H., Tetrahedron Asymmetry, 7, 2595–2602 (1996).

4. 4) Ono M., Zhao X. Y., Shida Y., Akita H., Tetrahedron, 63, 10140–10148 (2007).

5. 5) Numata A., Hokimoto K., Takemura T., Katsuno T., Yamamoto K., Chem. Pharm. Bull., 32, 2815–2820 (1984).

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