(E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis

(E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis

Bibliographic Details
Main Authors: Jyoti Chandra, Srinivasa Rao Manne, Sandip Mondal, Bhubaneswar Mandal
Format: Article
Language:English
Published: American Chemical Society 2018-06-01
Series:ACS Omega
Online Access:http://dx.doi.org/10.1021/acsomega.8b00732
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spelling doaj-67ec07c4feae430cb3e01603bdc7ce822020-11-25T01:57:38ZengAmerican Chemical SocietyACS Omega2470-13432018-06-01366120613310.1021/acsomega.8b00732(E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide SynthesisJyoti ChandraSrinivasa Rao ManneSandip MondalBhubaneswar Mandalhttp://dx.doi.org/10.1021/acsomega.8b00732
collection DOAJ
language English
format Article
sources DOAJ
author Jyoti Chandra
Srinivasa Rao Manne
Sandip Mondal
Bhubaneswar Mandal
spellingShingle Jyoti Chandra
Srinivasa Rao Manne
Sandip Mondal
Bhubaneswar Mandal
(E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
ACS Omega
author_facet Jyoti Chandra
Srinivasa Rao Manne
Sandip Mondal
Bhubaneswar Mandal
author_sort Jyoti Chandra
title (E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
title_short (E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
title_full (E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
title_fullStr (E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
title_full_unstemmed (E)‑Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis
title_sort (e)‑ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: a modified yamaguchi reagent for enantioselective esterification, thioesterification, amidation, and peptide synthesis
publisher American Chemical Society
series ACS Omega
issn 2470-1343
publishDate 2018-06-01
url http://dx.doi.org/10.1021/acsomega.8b00732
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AT srinivasaraomanne eethyl2cyano2246trichlorobenzoyloxyiminoacetateamodifiedyamaguchireagentforenantioselectiveesterificationthioesterificationamidationandpeptidesynthesis
AT sandipmondal eethyl2cyano2246trichlorobenzoyloxyiminoacetateamodifiedyamaguchireagentforenantioselectiveesterificationthioesterificationamidationandpeptidesynthesis
AT bhubaneswarmandal eethyl2cyano2246trichlorobenzoyloxyiminoacetateamodifiedyamaguchireagentforenantioselectiveesterificationthioesterificationamidationandpeptidesynthesis
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