Efficient and highly selective cyclization induced by Lewis acid to generate 2-hydroxyl-α-cyclogeraniol-Reference-Cited by-同舟云学术

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Efficient and highly selective cyclization induced by Lewis acid to generate 2-hydroxyl-α-cyclogeraniol

Published:2016-10-07 Issue:23 Volume:46 Page:1932-1939
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Wang Zi¹,Qi Weiyi²,Yan Yixuan³,Hu Youhong²,Song Linhua¹

Affiliation:

1. College of Science, China University of Petroleum (East China), Qingdao, China

2. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China

3. School of Pharmacy Lanzhou University, Lanzhou, Gansu, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2016.1239739

Reference8 articles.

1. A Simple and Efficient Highly Enantioselective Synthesis of α-Ionone and α-Damascone

2. First total synthesis of (+)-apotrisporin E and (+)-apotrientriols A–B: a cyclization approach to apocarotenoids

3. Lipase-mediated resolution of the hydroxy-cyclogeraniol isomers: application to the synthesis of the enantiomers of karahana lactone, karahana ether, crocusatin C and γ-cyclogeraniol

4. Taxol Total Synthesis: Preparation of a Chiral Ring A Moiety via Biomimetic Cyclization and Evaluation of a Tandem Nitrile Oxide Strategy for Rings B/C

5. Achilleol A: A new monocyclic triterpene skeleton from Achillea odorata L.

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