Ruthenium-Catalyzed Hydroalkynylative Cyclization of 1,6-Enynes Induced by Substituent Effects-Reference-Cited by-同舟云学术

Ruthenium-Catalyzed Hydroalkynylative Cyclization of 1,6-Enynes Induced by Substituent Effects

Published:2016-08-09 Issue:16 Volume:18 Page:4040-4043
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Rui¹,Ni Zhenjie¹,Giordano Laurent¹,Tenaglia Alphonse¹

Affiliation:

1. Aix Marseille Université, CNRS, Cent Marseille, iSm2, Marseille 13013, France

Funder

Ministère de l'Enseignement Supérieur et de la Recherche

Centre National de la Recherche Scientifique

China Scholarship Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01901

Reference50 articles.

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2. bHuguet, N.; Echavarren, A. M.InGold Catalysis—An Homogeneous Approach;Toste, F. D., Michelet, V., Eds.Imperial College Press:London, 2014; pp275–330.

3. Carbohydroxypalladation reactions in aqueous medium: An efficient route to 3-(1-hydroxyaryl)tetrahydrofurans

4. Cycloisomerization of 1,6-enynes in organoaqueous medium: an efficient and eco-friendly access to furan derivatives. Synthesis of a key intermediate of podophyllotoxin

5. Pd-catalyzed route to (±)-podophyllotoxin skeleton. Synthesis of the aryltetralin derivative

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