Topics in Current Chemistry
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1 220 Topics in Current Chemistry Editorial Board: A. de Meijere K. N. Houk H. Kessler J.-M. Lehn S.V. Ley S.L. Schreiber J. Thiem B.M. Trost F. Vogtle H. Yamamoto
2 Springer Berlin Heidelberg New York Barcelona Hong Kong London Milan Paris Tokyo
3 New Aspects in Phosphorus Chemistry I Volume Editor: Jean-Pierre Majoral With contributions by G. Bertrand, D. Bourissou, J.-M. Brunei, G. Buono, V. Cadierno, D. Carmichael, H. Dorn, M. Ehses, P. Guga, A. Igau, B. A. Kashemirov, J.-P. Majoral, I. Manners, F. Mathey, C. E. McKenna, A. R. Me Williams, A. Okruszek, M. Peruzzini, A. Romerosa, W. J. Stec, M. Zablocka Springer
4 The series Topics in Current Chemistry presents critical reviews of the present and future trends in modern chemical research. The scope of coverage includes all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the nonspecialist reader, whether at the university or in industry, a comprehensive overview of an area where new insights are emerging that are of interest to a larger scientific audience. As a rule, contributions are specially commissioned. The editors and publishers will, however, always be pleased to receive suggestions and supplementary information. Papers are accepted for Topics in Current Chemistry in English. In references Topics in Current Chemistry is abbreviated Top. Curr. Chem. and is cited as a journal. Springer WWW home page: Visit the TCC home page at or ISSN ISBN Springer- Verlag Berlin Heidelberg New York Library of Congress Catalog Card Number This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilm or in any other ways, and storage in data banks. Duplication of this publication or parts thereof is only permitted under the provisions of the German Copyright Law of September 9,1965, in its current version, and permission for use must always be obtained from Springer- Verlag. Violations are liable for prosecution under the German Copyright Law. Springer-Verlag Berlin Heidelberg New York a member of BertelsmannSpringer Science+Business Media GmbH Springer-Verlag Berlin Heidelberg 2002 Printed in Germany The use of general descriptive names, registered names, trademarks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. Cover design: Friedhelm Steinen-Broo, Barcelona; MEDIO, Berlin Typesetting: Fotosatz-Service Kohler GmbH, Wurzburg SPIN: /3020 ra Printed on acid-free paper
5 Volume Editor Dr. Jean-Pierre Majoral Directeur de Recherche Laboratoire de Chimie de Coordination du CNRS 205, route de Narbonne Toulouse, Cedex 4, France Editorial Board Prof. Dr. Armin de Meijere Institut fur Organische Chemie der Georg-August-Universitat Tammannstrafie Gottingen, Germany Prof. Dr. Horst Kessler Institut fur Organische Chemie TU Munchen Lichtenbergstrafie Garching, Germany kessler@ch.tum.de Prof. Steven V. Ley- University Chemical Laboratory Lensfield Road Cambridge CB2 1EW, Great Britain svllooo@cus.cam.ac.uk Prof. Dr. Joachim Thiem Institut fur Organische Chemie Universitat Hamburg Martin-Luther-King-Platz Hamburg, Germany E-maihthiem@chemie.uni-hamburg.de Prof. Dr. Fritz Vogtle Kekule-Institut fur Organische Chemie und Biochemie der Universitat Bonn Gerhard-Domagk-Strafie Bonn, Germany voegtle@uni-bonn.de Prof.K.N.Houk Department of Chemistry and Biochemistry University of California 405 Hilgard Avenue Los Angeles, CA , USA houk@chem.ucla.edu Prof. Jean-Marie Lehn Institut de Chimie Universite de Strasbourg 1 rue Blaise Pascal, B.P.Z 296/R Strasbourg Cedex, France lehn@chimie. u-strasbg.fr Prof. Stuart L. Schreiber Chemical Laboratories Harvard University 12 Oxford Street Cambridge, MA , USA sls@slsiris.harvard.edu Prof. Barry M. Trost Department of Chemistry Stanford University Stanford, CA , USA bmtrost@leland.stanford.edu Prof. Hisashi Yamamoto School of Engineering Nagoya University Chikusa, Nagoya , Japan j45988a@nucc. cc. nagoya-u.ac.jp
6 Topics in Current Chemistry Now Also Available Electronically For all customers with a standing order for Topics in Current Chemistry we offer the electronic form via LINK free of charge. Please contact your librarian who can receive a password for free access to the full articles by registration at: If you do not have a standing order you can nevertheless browse through the table of contents of the volumes and the abstracts of each article at: There you will also find information about the - Editorial Board - Aims and Scope - Instructions for Authors
7 Preface Undoubtedly the chemistry of phosphorus appears more and more attractive in the sense that phosphorus presents an extraordinary versatile behaviour that allows the synthesis of a large number of different phosphorus reagents usable for applications in different fields, from biology to material science without forgetting key applications in catalysis. The full maturity of this topic of research can be explained by all the acquired knowledge over these twenty last years. Organic and inorganic chemistries of P in, P ]V and P v species have been the subject of thousands of publications while the chemistry of low coordinated phosphorus derivatives experienced its hour of glory from the 1970s to the early 1990s. In parallel, interactions between phosphorus compounds and transition metals afforded many complexes, a lot of which present fascinating properties as catalysts. The interest in all these themes really is not decreasing, indeed some fascinating areas of research are emerging or are the subject of many investigations: the medicinal chemistry of bisphosphonates, the role of phosphorus in biology, phosphorus ligands in radiopharmaceutical chemistry, phosphorus in material science, new polymers and dendrimers incorporating phosphorus, and asymmetric catalysis to name but a few. Indeed researchers, benefitting from their background in basic phosphorus chemistry are developing many new fields of research. Therefore it appeared opportune not only to give an overview of the state of the art of the new aspects in phosphorus chemistry but also to try to draw what might be of interest for development in the future using phosphorus. This Topics in Current Chemistry volume starts with a comparison of carbon, nitrogen and phosphorus chemistry concerning the preparation and the properties of three-membered rings as neutral cationic or radical species (G. Bertrand et al.). The specificity of phosphorus is clearly shown. The following contribution by F. Mathey et al. reports new trends in phosphametallocene chemistry with emphasis on the applications of transition-metal phospholyl complexes in homogenous catalysis. How is it possible to take advantage of the properties of a given element to develop the chemistry of another one? This is what is shown in the contribution of J.-P. Majoral et al. describing the use of benzyne zirconocene reagents as tools in phosphorus chemistry. Trie use of phosphorus in catalysis is a topic impossible to circumvent. The review by G. Buono et al. highlights the role of new chiral organophosphorus catalysts in asymmetric synthesis.
8 VIII Preface One of the sources of phosphorus reagents is white phosphorus. All efforts to transform this bulk material are of great interest. M. Peruzzini et al. presents a critical survey of the coordination chemistry of white phosphorus, metal mediating the degradation and reaggregation of P 4. A survey of the chemistry and the role of phosphorus would not be complete without entering the world of material science and bioscience. Again, phosphorus has proved useful in these areas of research. Synthesis and properties of new inorganic polymers containing phosphorus and more specially poly(thionylphosphazenes), hybrids of "classical" polyphosphazenes and poly(oxothiazenes) are discussed among the preparation of a variety of novel polymeric materials by I. Manners et al. Synthetic methods leading to P-chiral oligonucleotides for which broad applications might be expected in biochemistry and molecular biology are presented in the contribution by W. Stec et al. Special emphasis has been put on the oxathiaphospholane methodology for the stereocontrolled synthesis of P-chiral biophosphate analogues. Recent advances in carbonylphosphonate chemistry are reported by C. E. McKenna et al. with emphasis on the synthesis, chemical properties and synthetic utility of this versatile class of organophosphorus compounds. In conclusion the present volume, the first of a series of volumes, gives a general and at the same time rather detailed review on the main research developments in phosphorus chemistry. There is still more to come, such a chemistry being so fascinating and so diversified. Toulouse, November 2001 Jean-Pierre Majoral
9 Contents Diphosphorus-Containing Unsaturated Three-Membered Rings: Comparison of Carbon, Nitrogen, and Phosphorus Chemistry G. Bertrand, D. Bourissou 1 New Trends in Phosphametallocene Chemistry D. Carmichael, F. Mathey 27 Benzyne-Zirconocene Reagents as Tools in Phosphorus Chemistry J.-P. Majoral, A. Igau, V. Cadierno, M. Zablocka 61 New Chiral Organophosphorus Catalysts in Asymmetric Synthesis J.M. Brunei, G.Buono 79 Metal-Mediated Degradation and Reaggregation of White Phosphorus M. Ehses, A. Romerosa, M. Peruzzini 107 New Inorganic Polymers Containing Phosphorus A. R. McWilliams, H. Dorn, I. Manners 141 Recent Advances in Stereocontrolled Synthesis of P-Chiral Analogues of Biophosphates P.Guga.A.Okruszek.W.J.Stec 169 Recent Progress in Carbonylphosphonate Chemistry C.E.McKenna,B.A.Kashemirov 201 Author Index Volumes
10 Contents of Volume 216 Stereoselective Heterocyclic Synthesis III Volume Editor: P. Metz ISBN X Stereoselective Intramolecular 1,3-Dipolar Cycloadditions I.N.N. Namboothiri, A. Hassner 4-Acetoxy- and 4-Cyano-l,3-Dioxanes in Synthesis ChJ. Sinz, S.C. Rychnovsky The Synthetic Potential of Three-Membered Ring Aza-Heterocycles B. Zwanenburg, P. ten Holte Synthesis of Medium-Sized Ring Lactams U. Nubbemeyer
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