Versatile Methodology to Hydrate Alkynes, in the Presence of a Wide Variety of Functional Groups, with Mercury(II) p-Toluensulfonamidate, Under Catalytic, Mild, and Neutral Conditions-Reference-Cited by-同舟云学术

Versatile Methodology to Hydrate Alkynes, in the Presence of a Wide Variety of Functional Groups, with Mercury(II) p-Toluensulfonamidate, Under Catalytic, Mild, and Neutral Conditions

Published:2013-04-28 Issue:15 Volume:43 Page:2062-2072
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Corominas Albert¹,Montaña Ángel M.¹

Affiliation:

1. a Unidad de Química Orgánica Industrial y Aplicada, Departamento de Química Orgánica, Facultad de Química , Universidad de Barcelona , Barcelona , Spain

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2012.686003

Reference16 articles.

1. Transition-Metal-Catalyzed Addition of Heteroatom−Hydrogen Bonds to Alkynes

2. Ueber eine neue Methode direkter Addition von Wasser (Hydratation) an die Kohlenwasserstoffe der Acetylenreihe

3. A new catalyst for organic synthesis: mercuric triflate

4. Mercuric Triflate-TMU Catalyzed Hydration of Terminal Alkyne to give Methyl Ketone under Mild Conditions

5. AU(I)-CATALYZED HYDRATION OF ALKYNES: 2,8-NONANEDIONE

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