γ-Alkylsulfide phosphonates through the thia-Michael strategy-Reference-Cited by-同舟云学术

γ-Alkylsulfide phosphonates through the thia-Michael strategy

Published:2014-09-01 Issue:6 Volume:35 Page:674-682
ISSN:1741-5993
Container-title:Journal of Sulfur Chemistry
language:en
Short-container-title:Journal of Sulfur Chemistry

Author:

Abdelli Abderrahmen¹²,M'rabet Hedi¹,Efrit Mohamed Lotfi¹,Gaucher Anne²,Prim Damien²

Affiliation:

1. Laboratoire de Synthèse Organique et Hétérocyclique, Université de Tunis El Manar-2092-Tunis, Tunisie

2. Institut Lavoisier de Versailles-UMR CNRS 8180, Université de Versailles-Saint-Quentin-en-Yvelines, 45, avenue des Etats-Unis, 78035 Versailles Cedex, France

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/17415993.2014.951856

Reference32 articles.

1. Synthesis and bioactivities of novel thioether/sulfone derivatives containing 1,2,3-thiadiazole and 1,3,4-oxadiazole/thiadiazole moiety

2. Plasticity in the copper–thioether bond: Manifestation in blue Cu proteins and in synthetic analogs

3. A novel environmentally friendly process for carbon–sulfur bond formation catalyzed by montmorillonite clays

4. Chiral Amino Ether-Controlled Catalytic Enantioselective Arylthiol Conjugate Additions to α,β-Unsaturated Esters and Ketones: Scope, Structural Requirements, and Mechanistic Implications

5. (Methylsulfanyl)alkanoate ester biosynthesis in Actinidia chinensis kiwifruit and changes during cold storage

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