Literature DB >> 15104470

Convenient and efficient reduction of 1,1'-binaphthyls to H8-1,1'-binaphthyl derivatives with Pd and Ru catalysts on solid support.

Andrei Korostylev1, Vitali I Tararov, Christine Fischer, Axel Monsees, Armin Börner.   

Abstract

Hydrogenation of chiral 2,2'-functionalized 1,1'-binaphthyls with Pd and Ru solid-supported metal catalysts was found to be a clean and convenient pathway to 5,5',6,6',7,7',8,8'-octahydro-1,1'-dinaphthyl derivatives. In most cases no racemization was observed in the course of the reaction.

Entities:  

Year:  2004        PMID: 15104470     DOI: 10.1021/jo0497609

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


  3 in total

1.  Steric modulation of chiral biaryl diamines via Pd-catalyzed directed C-H arylation.

Authors:  Christopher C Scarborough; Richard I McDonald; Caroline Hartmann; Graham T Sazama; Ana Bergant; Shannon S Stahl
Journal:  J Org Chem       Date:  2009-03-20       Impact factor: 4.354

2.  A new method for the synthesis of H(4)-BINOL.

Authors:  Lars V Heumann; Gary E Keck
Journal:  J Org Chem       Date:  2008-05-20       Impact factor: 4.354

3.  Multivariate approach for the enantioselective analysis in micellar electrokinetic chromatography-mass spectrometry. I. Simultaneous optimization of binaphthyl derivatives in negative ion mode.

Authors:  Jun He; Shahab A Shamsi
Journal:  J Chromatogr A       Date:  2008-12-06       Impact factor: 4.759

  3 in total

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