Se-(9-Fluorenylmethyl) Selenoesters; Preparation, Reactivity, and Use as Convenient Synthons for Selenoacids-Reference-Cited by-同舟云学术

Se-(9-Fluorenylmethyl) Selenoesters; Preparation, Reactivity, and Use as Convenient Synthons for Selenoacids

Published:2013-07-01 Issue:14 Volume:15 Page:3758-3761
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fécourt Fabien¹,Delpech Bernard¹,Melnyk Oleg¹,Crich David¹

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, CNRS, 1 Avenue de la Terrasse, 91190 Gif-sur-Yvette, France, CNRS UMR 8161, Univ. Lille Nord de France, Institut Pasteur de Lille, 59021, Lille, France, and Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401677a

Reference67 articles.

1. Thion (RCSOH), Selenon (RCSeOH), and Telluron (RCTeOH) Acids as Predominant Species

2. bKato, S.; Murai, T.InThe Chemistry of Acid Derivatives;Patai, S., Ed.Wiley:Chichester, 1992; Vol.2, pp803–847.

3. Rethinking amide bond synthesis

4. A simple synthesis of 2,2-disubstituted tetrahydrothiophenes

5. A convenient and highly chemoselective method for the reductive acetylation of azides

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