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Science of Synthesis Houben–Weyl Methods of Molecular Transformations www.science-of-synthesis.com 2003 Georg Thieme Verlag Rüdigerstrasse 14 D-70469 Stuttgart Copyright and all related rights reserved, especially the right of copying and distribution, multiplication and reproduction, as well as of translation. No part of this publication may be reproduced by any process, whether by photostat or microfilm or any other procedure, without previous written consent by the publisher. This also includes the use of electronic media of data processing on reproduction of any kind. If you have any queries or comments about the content of Science of Synthesis, please contact: Dr. M. Fiona Shortt de Hernandez Managing Editor Science of Synthesis/Houben–Weyl Thieme Chemistry Georg Thieme Verlag Rüdigerstrasse 14 D-70469 Stuttgart Phone: +49 711 8931-783 Fax: +49 711 8931-777 E-mail: fiona.shortt@thieme.de www.science-of-synthesis.com
Page 1: Science of Synthesis Houben-Weyl Me
Page 7 and 8: Table of Contents Preface .........
Page 9: Preface As our understanding of the
Page 12 and 13: 12 Science of Synthesis Category 1:
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Page 28 and 29: 28 Biographical Sketch John Montgom
Page 30 and 31: 30 1.1.3.4 Method 4: Coupling of Al
Page 32 and 33: 32 Science of Synthesis 1.1 Organom
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54 Science of Synthesis 1.1 Organom
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2003 Georg Thieme Verlag Rüdigerst
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2.6 Product Class 6: Organometallic
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2.6.8.5 Method 5: From Complexes Co
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2.6.1 Metal-Carbene Complexes 91 en
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2.6.1 Metal-Carbene Complexes 93 ri
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2.6.1 Metal-Carbene Complexes 95 ci
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2.6.1 Metal-Carbene Complexes 97 ar
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2.6.1 Metal-Carbene Complexes 99 of
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2.6.1 Metal-Carbene Complexes 101 p
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2.6.2 Metal-Carbyne Complexes 103 S
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2.6.2 Metal-Carbyne Complexes 105 N
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Scheme 16 Stoichiometric Alkyne Met
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2.6.2 Metal-Carbyne Complexes 109
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2.6.3 Metal-s-Alkyl and -s-Aryl Hom
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2.6.4 Metal-s-Alkyl and -s-Aryl Non
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2.6.5 Metallacyclic Complexes 121 p
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2.6.6 Complexes with Triply Bonded
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2.6.7 Complexes with Doubly Bonded
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2.6.8 Complexes with Singly Bonded
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2.6.9 Miscellaneous Complexes 133
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References 135 References [1] Coles
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References 137 [85] Allen, S. R.; B
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References 139 [176] Chisholm, M. H
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142
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144 Biographical Sketch Nicholas La
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146 4.4.27 Product Subclass 27: Æ-
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148 Science of Synthesis 4.4 Silico
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160 References [46] Hosomi, A.; And
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163 Science of Synthesis Houben-Wey
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5.1.22 Product Subclass 22: Aryl- a
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5.1.22 Aryl- and Heteroarylgermanes
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References 175 References [1] Heves
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Abbreviations Chemical Name Used in
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Chemical (cont.) Abbreviations 179
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Abbreviations 181 General absolute
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