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22 Science of Synthesis Category 1: Organometallics 5.2.28 Product Subclass 28: Allylstannanes R. L. Marshall 5.2.29 Product Subclass 29: Alkylstannanes D. Young 5.3 Product Class 3: Lead Compounds M. G. Moloney 5.3.1 Product Subclass 1: Lead Hydrides M. G. Moloney 5.3.2 Product Subclass 2: Diplumbenes and Diplumbanes N. Takeda, N. Tokitoh, and R. Okazaki 5.3.3 Product Subclass 3: Metalated Lead Compounds N. Takeda, N. Tokitoh, and R. Okazaki 5.3.4 Product Subclass 4: Organoplumbyl Oxides, Sulfides, Selenides, and Tellurides (Double Bonded) N. Takeda, N. Tokitoh, and R. Okazaki 5.3.5 Product Subclass 5: Plumbylenes N. Takeda, N. Tokitoh, and R. Okazaki 5.3.6 Product Subclass 6: Halo(organo)plumbanes P. J. Guiry and P. J. McCormack 5.3.7 Product Subclass 7: Organoplumboxanes and Related Compounds P. J. Guiry and P. J. McCormack 5.3.8 Product Subclass 8: Acyloxy(organo)plumbanes P. J. Guiry and P. J. McCormack 5.3.9 Product Subclass 9: Plumbyl Enol Ethers P. J. Guiry and P. J. McCormack 5.3.10 Product Subclass 10: Organoplumbane Sulfur Compounds P. J. Guiry and P. J. McCormack 5.3.11 Product Subclass 11: Organoplumbyl Selenides, Tellurides, and Related Compounds P. J. Guiry and P. J. McCormack 5.3.12 Product Subclass 12: Organoplumbanamines and Related Compounds P. J. Guiry and P. J. McCormack
Table of Contents 23 5.3.13 Product Subclass 13: Organoplumbyl Phosphines and Phosphine Oxides P. J. Guiry and P. J. McCormack 5.3.14 Product Subclass 14: Triorganolead Cyanides and Triorganolead Cyanates P. A. C. Eagle 5.3.15 Product Subclass 15: Acylplumbanes P. A. C. Eagle 5.3.16 Product Subclass 16: Lead Isocyanates, Isothiocyanates, Diazoplumbanes, and Iminoplumbanes P. A. C. Eagle 5.3.17 Product Subclass 17: 1- or 2-Alkoxy- and 1- or 2-(Alkylsulfanyl) and 1- or 2-Aminoalkenyl(triorgano)plumbanes P. A. C. Eagle 5.3.18 Product Subclass 18: 1-Halo-, 1-Alkoxy-, 1-Hydroxy-, and 1-Aminoalkylplumbanes P. A. C. Eagle 5.3.19 Product Subclass 19: Alkynylplumbanes P. A. C. Eagle 5.3.20 Product Subclass 20: Allenylplumbanes P. A. C. Eagle 5.3.21 Product Subclass 21: Arylplumbanes P. A. C. Eagle 5.3.22 Product Subclass 22: Vinylplumbanes P. A. C. Eagle 5.3.23 Product Subclass 23: Benzylplumbanes P. A. C. Eagle 5.3.24 Product Subclass 24: Allylplumbanes P. A. C. Eagle 5.3.25 Product Subclass 25: Alkylplumbanes P. A. C. Eagle
Page 1: Science of Synthesis Houben-Weyl Me
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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: Table of Contents 19 5.1.12 Product
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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
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Page 49 and 50: 1.1.3 Nickel-Alkyne Complexes 49 Ca
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Page 57 and 58: 1.1.3 Nickel-Alkyne Complexes 57 Sc
Page 59 and 60: 1.1.3 Nickel-Alkyne Complexes 59 en
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Page 63 and 64: 1.1.4 Nickel-Alkene Complexes 63 Bi
Page 65 and 66: 1.1.4 Nickel-Alkene Complexes 65 Sc
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1.1.4 Nickel-Alkene Complexes 73 1.
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1.1.4 Nickel-Alkene Complexes 75 4-
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1.1.4 Nickel-Alkene Complexes 77 1.
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References 79 References [1] Chetcu
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References 81 [98] Tsuda, T.; Mizun
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Science of Synthesis Houben-Weyl Me
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86 Biographical Sketches Rinaldo Po
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88 2.6.4.2.2 Variation 2: Two-Elect
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90 2.6 Product Class 6: Organometal
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92 Science of Synthesis 2.6 Complex
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100 Science of Synthesis 2.6 Comple
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141 Science of Synthesis Houben-Wey
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2002 Georg Thieme Verlag Rüdigerst
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4.4.27 Product Subclass 27: Æ-Halo
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4.4.27 Æ-Haloalkylsilanes 147 Sche
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4.4.27 Æ-Haloalkylsilanes 149 dros
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4.4.27 Æ-Haloalkylsilanes 151 4.4.
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4.4.27 Æ-Haloalkylsilanes 153 In g
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4.4.27 Æ-Haloalkylsilanes 155 4.4.
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4.4.27 Æ-Haloalkylsilanes 157 Æ-H
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References 159 References [1] Haman
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References 161 [93] Bruno, J. W.; S
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164
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166 Biographical Sketches Alan Spiv
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168 5.1.22 Product Subclass 22: Ary
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170 Science of Synthesis 5.1 German
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176 References [43] Eaborn, C.; Var
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178 Abbreviations Chemical (cont.)
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180 Abbreviations Ligands (cont.) 2
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182 Abbreviations General (cont.) q
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