ca01 only detailed ToC 1..24

More documents

Recommendations

Info

166 Biographical Sketches Alan Spivey received his BSc in chemistry in 1988 from the University of Nottingham, UK and his DPhil in 1991 from the University of Oxford under the guidance of Prof. Sir Jack Baldwin. After postdoctoral work at the UniversitØ de Gen›ve, Switzerland with the late Prof. Wolfgang Oppolzer, and at the University of Cambridge with Prof. Sir Alan Battersby, he moved to a lectureship at the University of Sheffield. In January 2003 he moved to Imperial College London as a reader. Research in his group is focused on the development of new catalysts for asymmetric acylation, new linkers for solid phase organic synthesis, chemical aspects of signal transduction, and total synthesis of bioactive natural products. Chris Diaper received his BSc in chemistry in 1996 from the University of Bradford, UK and his PhD in 2000 from the University of Sheffield under the supervision of Dr Alan Spivey. After postdoctoral work at the University of Nottingham with Prof. Gerry Pattenden he moved to his current position as a postdoctoral fellow at the University of Alberta, Canada working with Prof. John Vederas. His research interests include the development of germanium based linkers for solid-phase synthesis, the total synthesis of marine natural products and mechanistic aspects of the diaminopimelate (DAP)biosynthetic pathway.
5.1.22 Product Subclass 22: Aryl- and Heteroarylgermanes A. C. Spivey and C. M. Diaper 5.1.22 Product Subclass 22: Aryl- and Heteroarylgermanes ..................... 168 Synthesis of Product Subclass 22 .......................................... 170 5.1.22.1 Method 1:From Halogermanes by Substitution with Arylmetals ............. 170 5.1.22.1.1 Variation 1:Using Preformed Arylmetals ................................... 170 5.1.22.1.2 Variation 2:Using Barbier-Type Reactions .................................. 171 5.1.22.2 Method 2:From Aryl Halides by Palladium(0)-Mediated Coupling with Digermanes ......................................................... 171 5.1.22.3 Method 3:From Aryl Halides by Insertion of Dichlorogermylene ............. 172 5.1.22.4 Method 4:Heteroarylgermanes by Cycloaddition ........................... 173 Applications of Product Subclass 22 in Organic Synthesis ................... 174 5.1.22.5 Method 5:Arylgermanes as Linkers for Solid-Phase Synthesis ............... 174 167
Page 1:
Science of Synthesis Houben-Weyl Me
Page 5:
Page 8 and 9:
8 Science of Synthesis Category 1:
Page 11 and 12:
Volume 1: Compounds withTransition
Page 13 and 14:
Table of Contents Volume 2 13 Volum
Page 15 and 16:
Table of Contents 15 Volume 4: Comp
Page 17 and 18:
Table of Contents 17 4.4.27 Product
Page 19 and 20:
Page 21 and 22:
Page 23:
Page 27 and 28:
2001 Georg Thieme Verlag Rüdigerst
Page 29 and 30:
1.1 Product Class 1: Organometallic
Page 31 and 32:
1.1 Product Class 1: Organometallic
Page 33 and 34:
1.1.1 Nickel Complexes of 1,3-Diene
Page 35 and 36:
1.1.1 Nickel Complexes of 1,3-Diene
Page 37 and 38:
1.1.2 Nickel-Allyl Complexes 37 tra
Page 39 and 40:
1.1.2 Nickel-Allyl Complexes 39 Bis
Page 41 and 42:
1.1.2 Nickel-Allyl Complexes 41 App
Page 43 and 44:
1.1.2 Nickel-Allyl Complexes 43 NiC
Page 45 and 46:
1.1.2 Nickel-Allyl Complexes 45 Sch
Page 47 and 48:
1.1.2 Nickel-Allyl Complexes 47 Sch
Page 49 and 50:
1.1.3 Nickel-Alkyne Complexes 49 Ca
Page 51 and 52:
1.1.3 Nickel-Alkyne Complexes 51 (2
Page 53 and 54:
1.1.3 Nickel-Alkyne Complexes 53 Sc
Page 55 and 56:
1.1.3 Nickel-Alkyne Complexes 55 at
Page 57 and 58:
1.1.3 Nickel-Alkyne Complexes 57 Sc
Page 59 and 60:
1.1.3 Nickel-Alkyne Complexes 59 en
Page 61 and 62:
1.1.3 Nickel-Alkyne Complexes 61 of
Page 63 and 64:
1.1.4 Nickel-Alkene Complexes 63 Bi
Page 65 and 66:
1.1.4 Nickel-Alkene Complexes 65 Sc
Page 67 and 68:
1.1.4 Nickel-Alkene Complexes 67 1.
Page 69 and 70:
1.1.4 Nickel-Alkene Complexes 69 Sc
Page 71 and 72:
1.1.4 Nickel-Alkene Complexes 71 [5
Page 73 and 74:
Page 75 and 76:
1.1.4 Nickel-Alkene Complexes 75 4-
Page 77 and 78:
Page 79 and 80:
References 79 References [1] Chetcu
Page 81 and 82:
References 81 [98] Tsuda, T.; Mizun
Page 83:
Page 86 and 87:
86 Biographical Sketches Rinaldo Po
Page 88 and 89:
88 2.6.4.2.2 Variation 2: Two-Elect
Page 90 and 91:
90 2.6 Product Class 6: Organometal
Page 92 and 93:
92 Science of Synthesis 2.6 Complex
Page 94 and 95:
Page 96 and 97:
Page 98 and 99:
Page 100 and 101:
100 Science of Synthesis 2.6 Comple
Page 102 and 103:
Page 104 and 105:
Page 106 and 107:
Page 108 and 109:
Page 110 and 111:
Page 112 and 113:
Page 114 and 115:
Page 116 and 117: 116 Science of Synthesis 2.6 Comple
Page 141 and 142: 141 Science of Synthesis Houben-Wey
Page 143 and 144: 2002 Georg Thieme Verlag Rüdigerst
Page 145 and 146: 4.4.27 Product Subclass 27: Æ-Halo
Page 147 and 148: 4.4.27 Æ-Haloalkylsilanes 147 Sche
Page 149 and 150: 4.4.27 Æ-Haloalkylsilanes 149 dros
Page 151 and 152: 4.4.27 Æ-Haloalkylsilanes 151 4.4.
Page 153 and 154: 4.4.27 Æ-Haloalkylsilanes 153 In g
Page 155 and 156: 4.4.27 Æ-Haloalkylsilanes 155 4.4.
Page 157 and 158: 4.4.27 Æ-Haloalkylsilanes 157 Æ-H
Page 159 and 160: References 159 References [1] Haman
Page 161: References 161 [93] Bruno, J. W.; S
Page 164 and 165: 164
Page 168 and 169: 168 5.1.22 Product Subclass 22: Ary
Page 170 and 171: 170 Science of Synthesis 5.1 German
Page 176 and 177: 176 References [43] Eaborn, C.; Var
Page 178 and 179: 178 Abbreviations Chemical (cont.)
Page 180 and 181: 180 Abbreviations Ligands (cont.) 2
Page 182: 182 Abbreviations General (cont.) q
show all

ca01 only detailed ToC 1..24

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?