Highly Regio- and Stereoselective Hydrosilylation of Internal Thioalkynes under Mild Conditions-Reference-Cited by-同舟云学术

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Highly Regio- and Stereoselective Hydrosilylation of Internal Thioalkynes under Mild Conditions

Published:2015-03-17 Issue:19 Volume:54 Page:5632-5635
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Ding Shengtao,Song Li-Juan,Wang Yong,Zhang Xinhao,Chung Lung Wa,Wu Yun-Dong,Sun Jianwei

Funder

Hong Kong RGC

National Science Foundation of China

Shenzhen Science and Technology Innovation Committee

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201500372/fullpdf

Reference86 articles.

1. Uses of Silicon-Containing Compounds in the Synthesis of Natural Products

2. A New Hydrosilylation Mechanism—New Preparative Opportunities

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1. Nickel-catalyzed regiodivergent syn-hydrosilylation of disubstituted alkynes;Science Bulletin;2024-08

2. Chemo-, regio- and stereoselective access to polysubstituted 1,3-dienes via Nickel-catalyzed four-component reactions;Nature Communications;2024-06-28

3. Regiodivergent Synthesis of 4‐ and 5‐Sulfenyl Oxazoles from Alkynyl Thioethers;Chemistry – A European Journal;2024-06-26

4. Lewis Acid-Catalyzed Formal [4 + 2] Reaction of Alkynyl Sulfides and 2-Pyrones To Access Polysubstituted Aryl Sulfides;The Journal of Organic Chemistry;2024-05-08

5. Bond Dissociation Energy-Controlled Regioselectivity in Hydrofunctionalization;ACS Catalysis;2024-05-08

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