Literature DB >> 29712018

Stereoselective Nucleophilic Trifluoromethylation of N-(tert-Butylsulfinyl)imines by Using Trimethyl(trifluoromethyl)silane.

G K Surya Prakash1, Mihirbaran Mandal1, George A Olah1.   

Abstract

A very general reaction is presented to achieve the nucleophilic transfer of "CF3 " to chiral N-(tert-butylsulfinyl)imines in high yield and high stereoselectivity. Tetrabutylammonium difluorotriphenylsilicate (TBAT) functions as a fluoride source, and aromatic, heterocyclic, and aliphatic sulfinylimines react smoothly. The high stereoselectivity suggests that the reaction proceeds through an open transition state. TMS=trimethylsilyl.
Copyright © 2001 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  amines; asymmetric synthesis; imines; nucleophilic addition; sulfinamides

Year:  2001        PMID: 29712018     DOI: 10.1002/1521-3773(20010202)40:3<589::AID-ANIE589>3.0.CO;2-9

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Single enantiomer synthesis of α-(trifluoromethyl)-β-lactam.

Authors:  Václav Jurčík; Alexandra M Z Slawin; David O'Hagan
Journal:  Beilstein J Org Chem       Date:  2011-06-06       Impact factor: 2.883

2.  Asymmetric synthesis of propargylamines as amino acid surrogates in peptidomimetics.

Authors:  Matthias Wünsch; David Schröder; Tanja Fröhr; Lisa Teichmann; Sebastian Hedwig; Nils Janson; Clara Belu; Jasmin Simon; Shari Heidemeyer; Philipp Holtkamp; Jens Rudlof; Lennard Klemme; Alessa Hinzmann; Beate Neumann; Hans-Georg Stammler; Norbert Sewald
Journal:  Beilstein J Org Chem       Date:  2017-11-15       Impact factor: 2.883

  2 in total

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