Chemoselective and Odorless Transthioacetalization of Acetals Using α-Oxo-Ketene Dithioacetals as Thiol Equivalents-Reference-Cited by-同舟云学术

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Chemoselective and Odorless Transthioacetalization of Acetals Using α-Oxo-Ketene Dithioacetals as Thiol Equivalents

Published:2013-05-03 Issue:9 Volume:43 Page:1280-1286
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Yu Hai-Feng

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397911.2011.631075

Reference13 articles.

1. Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis

2. The role of 1,3-dithianes in natural product synthesis

3. Highly Efficient Transthioacetalization of O,O-Acetals Catalyzed by Indium(III) Chloride

4. The First Nonthiolic, Odorless 1,3-Propanedithiol Equivalent and Its Application in Thioacetalization

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1. Selective hydrolysis of α-oxo ketene N,S-acetals in water: switchable aqueous synthesis of β-keto thioesters and β-keto amides;Beilstein Journal of Organic Chemistry;2024-09-03

2. A straightforward and rapid synthesis of polydithioacetals in the presence of chlorodimethylsilane;Polymer Chemistry;2024

3. A new and efficient approach to 2-hydroxybenzophenone derivatives via [5C + 1C] annulation of α-alkenoyl-α-aroyl ketene dithioacetals and nitroalkanes;Tetrahedron;2021-09

4. 30.3.3.2 1,3-Dithiolanes (Update 2018);Knowledge Updates 2018/2;2018

5. DBSA-catalyzed hydrolysis of chain α-oxo ketene dithioacetals in water: Aqueous synthesis of β-ketothioesters;Synthetic Communications;2017-11-08

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