Ruthenium-Catalyzed Propargylic Substitution Reaction of Propargylic Alcohols with Thiols: A General Synthetic Route to Propargylic Sulfides-Reference-Cited by-同舟云学术

Ruthenium-Catalyzed Propargylic Substitution Reaction of Propargylic Alcohols with Thiols: A General Synthetic Route to Propargylic Sulfides

Published:2002-11-23 Issue:51 Volume:124 Page:15172-15173
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Inada Youichi¹,Nishibayashi Yoshiaki¹,Hidai Masanobu¹,Uemura Sakae¹

Affiliation:

1. Department of Energy and Hydrocarbon Chemistry, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan, and Department of Materials Science and Technology, Science University of Tokyo, Noda, Chiba 278-8510, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja027754t

Reference19 articles.

1. Novel Propargylic Substitution Reactions Catalyzed by Thiolate-Bridged Diruthenium Complexes via Allenylidene Intermediates

2. Ruthenium-Catalyzed Propargylic Alkylation of Propargylic Alcohols with Ketones: Straightforward Synthesis of γ-Keto Acetylenes

3. Ruthenium-Catalyzed Propargylation of Aromatic Compounds with Propargylic Alcohols

4. Cyclization of Terminal Diynes Catalyzed by Thiolate-Bridged Diruthenium Complexes: A Simple Synthetic Route toendo-Macrocyclic (Z)-1-En-3-ynes

5. Copper(I)-Catalyzed Amination of Propargyl Esters. Selective Synthesis of Propargylamines, 1-Alken-3-ylamines, and (Z)-Allylamines

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