Chiral Sulfur Ligands: Asymmetric Catalysis

Author:   Hélène Pellissier (CNRS, France) ,  James J Spivey
Publisher:   Royal Society of Chemistry
Volume:   Volume 2
ISBN:  

9781847559241


Pages:   402
Publication Date:   01 October 2009
Format:   Hardback
Availability:   In Print   Availability explained
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Chiral Sulfur Ligands: Asymmetric Catalysis


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Overview

The goal of this book is to show the high potential of chiral sulfur-containing ligands to promote numerous asymmetric catalytic transformations. The important number of reports appeared in the literature over the last 35 years often highlighted spectacular results in terms of efficiency and enantioselectivity, allowing access to many biologically important molecules, which clearly demonstrates that these ligands can now be recognised as real competitors to the more usual phosphorus- or nitrogen-containing ligands. A key point of reference for post-graduate students, researchers and academics.

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Author:   Hélène Pellissier (CNRS, France) ,  James J Spivey
Publisher:   Royal Society of Chemistry
Imprint:   Royal Society of Chemistry
Volume:   Volume 2
Dimensions:   Width: 15.60cm , Height: 2.20cm , Length: 23.40cm
Weight:   1.628kg
ISBN:  

9781847559241


ISBN 10:   1847559247
Pages:   402
Publication Date:   01 October 2009
Audience:   College/higher education ,  Professional and scholarly ,  Tertiary & Higher Education ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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Hélène Pellissier was born in Gap, France. She carried out her PhD under the supervision of Dr G. Gil in Marseille and then entered the Centre National de la Recherche Scientifique in 1988. After a postdoctoral position in Professor K. P. C. Vollhardt's group at Berkeley, she joined the group of Professor M. Santelli in Marseille in 1992. Here she focused on the chemistry of BISTRO and its large application in organic synthesis.

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