Literature DB >> 18754577

Thioimides: new reagents for effective synthesis of thiolesters from carboxylic acids.

Adam Henke1, Jiri Srogl.   

Abstract

Thioimides and carboxylic acids are used as the precursors for the convenient synthesis of thiolesters in the phosphine mediated process. Cyclic and acyclic thioimides show equal efficiency, furnishing the desired thiolesters in good to excellent yields. The general, highly efficient transformation tolerates various functional groups and the resulting thiolesters are obtained in high purity after a simple separation. The reaction scope has been demonstrated on the preparation of several highly functionalized target molecules.

Entities:  

Year:  2008        PMID: 18754577     DOI: 10.1021/jo801319x

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  New class of biodegradable polymers formed from reactions of an inorganic functional group.

Authors:  Jun Yoo; Denison J Kuruvilla; Sheetal R D'Mello; Aliasger K Salem; Ned B Bowden
Journal:  Macromolecules       Date:  2012-02-21       Impact factor: 6.057

2.  Covalent Occlusion of the RORγt Ligand Binding Pocket Allows Unambiguous Targeting of an Allosteric Site.

Authors:  Femke A Meijer; Maxime C M van den Oetelaar; Richard G Doveston; Ella N R Sampers; Luc Brunsveld
Journal:  ACS Med Chem Lett       Date:  2021-03-08       Impact factor: 4.345

  2 in total

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