Andere Kunden interessierten sich auch für
![Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins]( "Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins")
Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins126,99 €![Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis]( "Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis")
Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis220,99 €![New Aspects in Phosphorus Chemistry IV]( "New Aspects in Phosphorus Chemistry IV")
New Aspects in Phosphorus Chemistry IV147,99 €![Battery Hazards and Accident Prevention]( "Battery Hazards and Accident Prevention")
Battery Hazards and Accident Prevention110,99 €![31P and 13C NMR of Transition Metal Phosphine Complexes]( "31P and 13C NMR of Transition Metal Phosphine Complexes")
31P and 13C NMR of Transition Metal Phosphine Complexes83,99 €![The Chemistry of Organophosphorus Compounds I]( "The Chemistry of Organophosphorus Compounds I")
The Chemistry of Organophosphorus Compounds I42,99 €![Metal Complexes with Tetrapyrrole Ligands III]( "Metal Complexes with Tetrapyrrole Ligands III")
Metal Complexes with Tetrapyrrole Ligands III37,99 €
Organolithium chemistry occupies a central position in the selective construction of C-C bonds in both simple and complex molecules. Paralleling the surge of interest in methods for asymmetric synthesis, the use of organolithiums in enantioselective synthesis has witnessed spectacular advances in a little over a decade. This volume is the first dedicated to a comprehensive coverage of this important area. It is designed to provide graduate students and researchers with a rich source of essential information on synthesising molecules in an enantioselective manner using organolithiums, and be an inspiration for future developments. Following an overview chapter summarising the key milestones, successive chapters, each written by leading experts in their field, critically survey all the major areas of progress.
This book is a valuable addition to the Topics in Organo-metallic
Chemistry series that has successfully culled a vast
topic into engaging and focused chapters through skillful
editorship. With minimal redundancy, the short text provides
comprehensive coverage of stereoselective deprotonations using
alkyllithiums in the presence of sparteine; the presentation
balances uninspiring examples with those in which the effectiveness
of the asymmetric depronation strategy is unsur-passed.
Interspersed throughout are complementary methods for
the creation and utilization of organolithiums in myriad reactions
that contribute meaningfully to the usefulness of the text. Clear
chapter headings and subject/author indexes make finding
information easy, and the volume will be a useful addition to
library reference collections.
Brian L. Pagenkopf, University of Texas at Austin
J. Am. Chem. Soc. 2003
To cover this very large subject, which has grown in size over several
decades and continues to develop rapidly, in such a compact form, as in this
volume, was certainly a demanding task, but it has been done successfully.
Through the sensible choice of topic areas and by the arrangement of the
material under different headings, the reader is given easy access to this complex subject.
Bernd Goldfuss
Institut für Organische Chemie
Universität Köln
Angewandte Chemie Int. Ed. 2004, 43, 778-781
www.angewandte.org
2004 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
------
In this monograph, which is the newest addition to the excellent Topics in Organometallic Chemistry series, several authors from eight research groups around the world describe the current state of the art in the area of stereoselectivity control using organolithium reagents.
This book is a fine addition to any collection of synthetic monographs or to a library centering on organometallicreactions. Practitioners of stereoselective synthesis of natural products will likely find it very useful.
Marek Majewski
University of Saskatchewan, Canada
Adv. Synth. Catal. 2005, 347, 719-720
Wiley-VCH
Chemistry series that has successfully culled a vast
topic into engaging and focused chapters through skillful
editorship. With minimal redundancy, the short text provides
comprehensive coverage of stereoselective deprotonations using
alkyllithiums in the presence of sparteine; the presentation
balances uninspiring examples with those in which the effectiveness
of the asymmetric depronation strategy is unsur-passed.
Interspersed throughout are complementary methods for
the creation and utilization of organolithiums in myriad reactions
that contribute meaningfully to the usefulness of the text. Clear
chapter headings and subject/author indexes make finding
information easy, and the volume will be a useful addition to
library reference collections.
Brian L. Pagenkopf, University of Texas at Austin
J. Am. Chem. Soc. 2003
To cover this very large subject, which has grown in size over several
decades and continues to develop rapidly, in such a compact form, as in this
volume, was certainly a demanding task, but it has been done successfully.
Through the sensible choice of topic areas and by the arrangement of the
material under different headings, the reader is given easy access to this complex subject.
Bernd Goldfuss
Institut für Organische Chemie
Universität Köln
Angewandte Chemie Int. Ed. 2004, 43, 778-781
www.angewandte.org
2004 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
------
In this monograph, which is the newest addition to the excellent Topics in Organometallic Chemistry series, several authors from eight research groups around the world describe the current state of the art in the area of stereoselectivity control using organolithium reagents.
This book is a fine addition to any collection of synthetic monographs or to a library centering on organometallicreactions. Practitioners of stereoselective synthesis of natural products will likely find it very useful.
Marek Majewski
University of Saskatchewan, Canada
Adv. Synth. Catal. 2005, 347, 719-720
Wiley-VCH