ca01 only detailed ToC 1..24

More documents

Recommendations

Info

88 2.6.4.2.2 Variation 2: Two-Electron Oxidative Additions .......................... 114 2.6.4.3 Method 3: By Oxidative Addition of Alkanes and Arenes ............... 115 2.6.4.4 Method 4: By Protonation of Carbene and Carbyne Ligands ............ 116 Applications of Product Subclass 4 in Organic Synthesis .................... 116 2.6.4.5 Method 5: Addition of Organochromium(III) Compounds to Carbonyl Compounds ..................................... 117 2.6.4.5.1 Variation 1: Reaction of Organochromium(III) Compounds Prepared from Organochromium(III) Chloride by Transmetalation ..... 117 2.6.4.5.2 Variation 2: Reaction of Organochromium(III) Compounds Prepared from Chromium(II) Chloride by Oxidative Addition (The Nozaki–Hiyama–Kishi Procedure) ..................... 118 2.6.4.5.3 Variation 3: Catalytic Nozaki–Hiyama–Kishi Reaction (The Fürstner Procedure) .................................. 119 2.6.4.6 Method 6: Additive–Reductive Carbonyl Dimerization ................. 119 2.6.5 Product Subclass 5: Metallacyclic Complexes ............................ 120 Synthesis of Product Subclass 5 ........................................... 121 2.6.5.1 Method 1: By Transmetalation ........................................ 121 2.6.5.2 Method 2: By Reductive Coupling of Alkenes .......................... 122 2.6.5.3 Method 3: By Addition of Alkenes to Carbene Complexes .............. 123 2.6.6 Product Subclass 6: Complexes with Triply Bonded Heteroelement Ligands .................................................. 123 2.6.7 Product Subclass 7: Complexes with Doubly Bonded Heteroelement Ligands .................................................. 124 Synthesis of Product Subclass 7 ........................................... 125 2.6.7.1 Method 1: From Complexes Containing Singly Bonded Heteroelement Ligands ................................... 125 2.6.7.2 Method 2: From Other Complexes Containing Doubly Bonded Heteroelement Ligands ................................... 126 2.6.7.3 Method 3: From Complexes Containing Triply Bonded Heteroelement Ligands ................................... 127 2.6.7.4 Method 4: By Oxidative Processes .................................... 128 Applications of Product Subclass 7 in Organic Synthesis .................... 129 2.6.7.5 Method 5: Catalytic Epoxidation of Alkenes ........................... 129 2.6.8 Product Subclass 8: Complexes with Singly Bonded Heteroelement Ligands .................................................. 130 Synthesis of Product Subclass 8 ........................................... 130 2.6.8.1 Method 1: By Oxidative Addition of Compounds with Single Bonds between Heteroelements ................................. 130 2.6.8.2 Method 2: By Transmetalation ........................................ 131 2.6.8.3 Method 3: From ó-Alkyl Complexes ................................... 131 2.6.8.4 Method 4: From Carbene or Carbyne Complexes ...................... 132
2.6.8.5 Method 5: From Complexes Containing Doubly Bonded Heteroelement Ligands ................................... 133 2.6.9 Product Subclass 9: Miscellaneous Complexes ........................... 133 Synthesis of Product Subclass 9 ........................................... 133 2.6.9.1 Method 1: Allylidene Complexes from Cyclopropenes ................. 133 89
Page 1:
Science of Synthesis Houben-Weyl Me
Page 5:
Science of Synthesis Houben-Weyl Me
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 75 and 76: 1.1.4 Nickel-Alkene Complexes 75 4-
Page 79 and 80: References 79 References [1] Chetcu
Page 81 and 82: References 81 [98] Tsuda, T.; Mizun
Page 83: Science of Synthesis Houben-Weyl Me
Page 86 and 87: 86 Biographical Sketches Rinaldo Po
Page 90 and 91: 90 2.6 Product Class 6: Organometal
Page 92 and 93: 92 Science of Synthesis 2.6 Complex
Page 100 and 101: 100 Science of Synthesis 2.6 Comple
Page 138 and 139:
138 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 166 and 167:
166 Biographical Sketches Alan Spiv
Page 168 and 169:
168 5.1.22 Product Subclass 22: Ary
Page 170 and 171:
170 Science of Synthesis 5.1 German
Page 172 and 173:
Page 174 and 175:
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

Create successful ePaper yourself

Delete template?

Save as template?