Water Enables Direct Use of Allyl Alcohol for Tsuji−Trost Reaction without Activators-Reference-Cited by-同舟云学术

Water Enables Direct Use of Allyl Alcohol for Tsuji−Trost Reaction without Activators

Published:2004-10-01 Issue:22 Volume:6 Page:4085-4088
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kinoshita Hidenori¹,Shinokubo Hiroshi¹,Oshima Koichiro¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan, and Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol048207a

Reference17 articles.

1. Palladium-catalyzed allylic alkylation of carbonucleophiles witl allylic borates or allylic alcohols and boron oxide under neutral conditions

2. Palladium-Catalyzed Etherification of Allyl Alcohols Using Phenols in the Presence of Titanium(IV) Isopropoxide

3. Et3B-promoted, Pd(0)-catalyzed allylation of active methylene compounds with allylic alcohols

4. Allylic alcohols as substrates for the palladium(0)-catalyzed allylic substitution

5. Palladium mediated allylic mitsunobu displacement: stereocontrolled synthesis of hepoxilin A3 and trioxilin A3 methyl esters

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