Literature DB >> 29711023

Amine Additives Greatly Expand the Scope of Asymmetric Hydrosilylation of Imines.

Xavier Verdaguer1, Udo E W Lange1, Stephen L Buchwald1.   

Abstract

Slow addition of a primary amine to the reaction mixture greatly increases the scope of the titanium-catalyzed asymmetric reduction of imines 1. An important added feature of this method is that chiral secondary amines 2 can be obtained in much higher optical purity (up to 99 % ee) than would be predicted from the E:Z ratios of the starting imines 1. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  Amines; Asymmetric catalysis; Imines; Reductions; Titanium

Year:  1998        PMID: 29711023     DOI: 10.1002/(SICI)1521-3773(19980504)37:8<1103::AID-ANIE1103>3.0.CO;2-M

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


  3 in total

1.  Click chemistry enables quantitative chiroptical sensing of chiral compounds in protic media and complex mixtures.

Authors:  F Yushra Thanzeel; Kaluvu Balaraman; Christian Wolf
Journal:  Nat Commun       Date:  2018-12-14       Impact factor: 14.919

2.  Early Main Group Metal Catalysts for Imine Hydrosilylation.

Authors:  Holger Elsen; Christian Fischer; Christian Knüpfer; Ana Escalona; Sjoerd Harder
Journal:  Chemistry       Date:  2019-10-16       Impact factor: 5.236

Review 3.  Enantioselective hydrogenations with chiral titanocenes.

Authors:  Oleksiy Vassylyev; Anthony Panarello; Johannes G Khinast
Journal:  Molecules       Date:  2005-07-14       Impact factor: 4.411

  3 in total

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