Rhodium Catalyzed Hydroformylation - INDEX

8/12/2019 Rhodium Catalyzed Hydroformylation - INDEX

1/9


2/9

282

This page has been reformatted by Knovel to provide easier navigation.

Index Terms Links

catalyst preparation 17 195 233 234catalyst recovery 210 211 212 213 214 215

216catalyst separation 256chelation control 134chiral cooperativity 116chiral diphosphines 131chiral diphosphites 109CHIRAPHOS 134CO dissociation 74 93 100 101 102cone angle 8 9 40continuous flow system 261 269

cooperative effect 131cosolvents 200cyclodextrins 275

D EGUPHOS 134dendrimer supported catalysts 268detergent alcohols 223detergents 201deuterioformylation 16 24 25 26 27 30

31 33 65 84dihydrofurans 150dihydropyrans 151dimer formation rhodium complexes 54 64 72 247dimethoxyacrolein 153dimethylbut-1-ene 18 25dinuclear species 137DIOCOL 133DIOP 2 78 82 84 133

dioxaphosphepine 120DIPAMP 2 4diphosphines as ligands 76-102 131 132 133 134 135

136 137 138 139 140diphosphites as ligands 44-59 108-120dirhodium species 54 65 69 137dissociation of CO 74 93 100 101 102distillative separation 2141,1-disubstituted alkenes 149 164dormant sites 247double-bond isomerization 207DPBS 219DPPB, dppb 217DuPhos 3 4

E conomics 198 204electron withdrawing substituents 38 85electronic effects 67 79 85 86 87 89
http://1155_02.pdf/http://1155_07.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_09.pdf/http://1155_06.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_02.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_10.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_07.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_01.pdf/http://1155_05.pdf/http://1155_01.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_02.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_06.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_07.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_02.pdf/


3/9

283


Index Terms Links

electronic parameter 8electron-withdrawing phosphines 79enantiofacial selection 128energetics 100 101 102ethyl acrylate 139 154evaporation 211 212 213 214extraction 211 215 216 217 218 219

220 225extraction after one-phase reaction 216

F errocene diphosphine ligands 79fluorous biphase catalysis 190 265fluxional behavior 114

G as recycle process 213glucal 158 167glucopyranose 123

H eavy-ends 207Heck mechanism 64heteroatom-directed

hydroformylation 160-hydride elimination 41 80 101 102hydroaminomethylation 172 177hydrocyanation 1 121hydrolysis phosphites 44

Immobilization 129 201immobilized aqueous phase 260in situ IR reflectance spectroscopy 68in situ IR transmission spectroscopy 28 68 69 90 138in situ NMR spectroscopy 49 50 51 52 68 69

80 91indicator ligand 39internal alkenes 55 56 57 58 59 95

263 275IR spectroscopic studies 43

J osiphos 4

K inetic studies 43 47 69 70 71 72

97 98 99 100 101 102

112kinetics two-phase catalysis 193 194 195kinetics, fluorous phase 266
http://1155_01.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_01.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_10.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_07.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_01.pdf/


4/9

284


Index Terms Links

L igand effects 1 2 3 4 5 6

7 8 9 10 11 12

13 14 38 66 67 6876-99

ligand loss 209 235 236 237 238 239240 241 242 243 244 245246

liquid recycle process 213long chain alkenes 200

Manufacturing cost 204mechanistic studies 22 40 41 42 43 44

48 49 50 51 52 5354 55 68 69 70 7172 96 97 98 99 113

114 115 116 117 118 119120 124 138

metal plating 235metalation 240 248

methyl methacrylate 5methyl oleate 55 56 573-methylpentane-1,5-diol 39micellar catalysis 256monophosphines as ligands 63 64 65 66 67 68

69 70 71 72 73 7475

monophosphites as ligands 37 38 39 40 41 4243 44 121

muscone 149

N anofiltration 268NAPHOS 137 193natural bite angle 82 88 96 97 98 99NMP 220NMR spectroscopy 49 50 51 52 68 69

80 91nylon monomers 226

O rganic synthesis, hydroformylationin 145orthometallation 54 55 210 240oxidation of phosphorus ligands 209 235 236 237
http://1155_01.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_02.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_09.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_01.pdf/


5/9

285


Index Terms Links

P -C bond cleavage 209 237 238 239 240 2413-pentenoate esters 58 227

pH aqueous phase catalysis 195phase transfer 275phase-transfer catalyst 225phosphine ligands 63-100phosphine-phosphite ligands 129 130 131

phosphites 35-61 109 -124 phospholes 67 82phosphonium intermediates 242phosphonium salt 210phosphorus ligand effects 1phyllantocin 162platinum systems 107 132P-O bond splitting 210polyketone 4polymer bound bulky phosphite 40polymer supported catalysts 269 270 271 272 273 274

process aspects 196 197 198 203- 227

propanal 200pyrrole 174

Q uaternary phosphonium salts 210

R affinate-II 197 220regioselectivity 72 73 74 75 96 97

98 99Reppe chemistry 1resting state 40 41 42 43 69 70

71 72 74 81 96 113138

rhodium containment 208rhodium leaching 208rhodium plating 208rhodium price 204ribose 122Ruhrchemie Rhne-Poulenc-Process 191 196

S ilica immobilized systems 273silylenol ethers 176silylformylation 178 181smart polymers 273
http://1155_08.pdf/http://1155_09.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_09.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_10.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_06.pdf/http://1155_06.pdf/http://1155_10.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_09.pdf/http://1155_06.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_10.pdf/http://1155_06.pdf/http://1155_06.pdf/http://1155_10.pdf/http://1155_07.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_07.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_09.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_10.pdf/http://1155_07.pdf/http://1155_03.pdf/http://1155_08.pdf/


6/9

286


Index Terms Links

sol-gel process 271solution structures 49 50 51 52 68 69

80 91 111 113 137standard conditions 70steric effects 38 40 46 68 113 114

115 116 117 118 119 120stripping reactor 212

styrene 18 20 21 26 30 107- 142substituted alkenes 55 56 57 58 59substrate-directed stereoselectivity 155sugar derivatives 121

sulfonated ligands 256 257 258 259 260 261262

supercritical fluids 262 263supported aqueous phase catalysis 260supramolecular catalysis 274

T erpenes 167Tischenko reaction 207

tpp 6 63 64 65 66 6768 69 70 71 72 7374 75 212 213 221

tppms 5 7 221tppts 5 6 7 191 215 221TPPTS, see tpptstransition state geometry 98trifluoropropene 18 153triphenyl phosphite 38triphenylphosphine, see tpptris(ortho tert -butylphenyl)phosphite 37 38 39 40 41 42

43 44 221tris(2,2,2-trifluoroethyl) phosphite 38tum-stile mechanism 53 114 138two-phase catalysis 190two-phase reaction 215

U nmodified rhodium catalysts 15 16 17 18 19 2021 22 23 24 25 2627 28 29 30 31 3233

V inyl acetate 18 20 vinyl arenes 152vinyl aromatics 107vinyl esters 150vinylpyridine 18 153
http://1155_10.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_06.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_01.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_02.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_03.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_03.pdf/http://1155_07.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_08.pdf/http://1155_03.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_08.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_06.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_06.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_02.pdf/http://1155_08.pdf/http://1155_07.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_01.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_01.pdf/http://1155_08.pdf/http://1155_06.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_06.pdf/http://1155_03.pdf/http://1155_02.pdf/http://1155_08.pdf/http://1155_05.pdf/http://1155_03.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_03.pdf/http://1155_10.pdf/


7/9

287


Index Terms Links

vinylpyrrole 153

W ilkinson 64 72Wittig reaction 177

X antphos ligands 87 88 89 90 91 9293 94 95 147 201 259

262 273xylofuranose 122
http://1155_06.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_07.pdf/http://1155_10.pdf/http://1155_10.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_07.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_05.pdf/http://1155_10.pdf/http://1155_04.pdf/http://1155_04.pdf/http://1155_06.pdf/http://1155_04.pdf/http://1155_06.pdf/


8/9

Catalysis by Metal Complexes

Series Editors:R. Ugo, University of Milan, Milan, ItalyB. R. James, University of British Columbia, Vancouver, Canada

1*. F. J. McQuillin: Homogeneous Hydrogenation in Organic Chemistry. 1976ISBN 90 -277 -0646 -8

2. P. M. Henry: Palladium Catalyzed Oxidation of Hydrocarbons. 1980ISBN 90 -277 -0986 -6

3. R. A. Sheldon: Chemicals from Synthesis Gas. Catalytic Reactions of CO andH2. 1983 ISBN 90 -277 -1489 -4

4. W. Keim (ed.): Catalysis in C1 Chemistry. 1983 ISBN 90 -277 -1527 -0

5. A. E. Shilov: Activation of Saturated Hydrocarbons by Transition Metal Com - plexes. 1984 ISBN 90 -277 -1628 -5

F. R. Hartley: Supported Metal Complexes. A New Generation of Catalysts. 19856.ISBN 90 -277 -1855 -5

7. Y. Iwasawa (ed.): Tailored Metal Catalysts. 1986 ISBN 90 -277 -1866 -0

8. R. S. Dickson: Homogeneous Catalysis with Compounds of Rhodium and lridium.1985 ISBN 90 -277 -1880 -6

9.G. Strukul (ed.): Catalytic Oxidations with Hydrogen Peroxide as Oxidant. 1993

ISBN 0 -7923 -1771 -8

A. Mortreux and F. Petit (eds.): Industrial Applications of Homogeneous Cata-10.lysis. 1988 ISBN 90 -277 -2520 -9

11 . N. Farrell: Transition Metal Complexes as Drugs and Chemotherapeutic Agents.1989 ISBN 90 -277 -2828 -3

12. A. F. Noels, M. Graziani and A. J. Hubert (eds.): Metal Promoted Selectivity inOrganic Synthesis. 199 1 ISBN 0 -7923 -1184 -1

L. I. Simndi: Catalytic Activation of Dioxygen by Metal Complexes. 199213.ISBN 0 -7923 -1896 -X

14. K. Kalyanasundaram and M. Grtzel (eds.), Photosensitization and Photocata-lysis Using Inorganic and Organometallic Compounds. 1993

P. A. Chaloner, M. A. Esteruelas, F. Jo and L. A. Oro: Homogeneous Hydrogen -ISBN 0 -7923 -2261 -4

15.ation. 1994 ISBN 0 -7923 -2474 -9


9/9

Catalysis by Metal Complexes16. G. Braca (ed.): Oxygenates by Homologation or CO Hydrogenation with Metal

Complexes. 1994 ISBN 0 -7923 -2628 -8F. Montanari and L. Casella (eds.): Metalloporphyrins Catalyzed Oxidations.

P.W.N.M. van Leeuwen, K. Morokuma and J.H. van Lenthe (eds.): Theoretical Aspects of Homogeneous Catalysis. Applications of Ab Initio Molecular Orbital

T. Funabiki (ed.): Oxygenases and Model Systems. 1997 ISBN 0 -7923 -4240 -2S. Cenini and F. Ragaini: Catalytic Reductive Carbonylation of Organic Nitro

A.E. Shilov and G.P. Shulpin: Activation and Catalytic Reactions of Saturated Hydrocarbons in the Presence of Metal Complexes. 2000

P.W.N.M. van Leeuwen and C. Claver (eds.): Rhodium Catalyzed Hydroformyla -

17.

1994 ISBN 0 -7923 -2657 -118.

Theory. 1995 ISBN 0 -7923 -3107 -919.

20.Compounds. 1997 ISBN 0 -7923 -4307 -7

21.

ISBN 0 -7923 -6101 -622.

tion. 2000 ISBN 0 -7923 -6551 -8

KLUWER ACADEMIC PUBLISHERS DORDRECHT / BOSTON / LONDON

*Volume I is previously published under the Series Title: Homogeneous Catalysis in Organic and Inorganic Chemistry.

Documents

Rhodium Catalyzed Hydroformylation - INDEX