Dehydrative Allylation of Alcohols and Deallylation of Allyl Ethers Catalyzed by [CpRu(CH3CN)3]PF6and 2-Pyridinecarboxylic Acid Derivatives. Effect of π-Accepting Ability and COOH Acidity of Ligand on Reactivity-Reference-Cited by-同舟云学术

Dehydrative Allylation of Alcohols and Deallylation of Allyl Ethers Catalyzed by [CpRu(CH3CN)3]PF6and 2-Pyridinecarboxylic Acid Derivatives. Effect of π-Accepting Ability and COOH Acidity of Ligand on Reactivity

Published:2009-02-05 Issue:2 Volume:38 Page:188-189
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Tanaka Shinji,Saburi Hajime,Hirakawa Takuya,Seki Tomoaki,Kitamura Masato

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference8 articles.

1. Catalytic Dehydrative Allylation of Alcohols

2. [CpRu(IV)(π-C3H5)(2-quinolinecarboxylato)]PF6 Complex: A Robust Catalyst for the Cleavage and Formation of Allyl Ethers

3. CpRuIIPF6/Quinaldic Acid-Catalyzed Chemoselective Allyl Ether Cleavage. A Simple and Practical Method for Hydroxyl Deprotection

4. Catalytic Removal of N-Allyloxycarbonyl Groups Using the [CpRu(IV)(π-C3H5)(2-quinolinecarboxylato)]PF6 Complex. A New Efficient Deprotecting Method in Peptide Synthesis

5. Highly reactive and chemoselective cleavage of allyl esters using an air- and moisture-stable [CpRu(IV)(π-C3H5)(2-quinolinecarboxylato)]PF6 catalyst

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