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Patai S. — The Chemistry of Organic Silicon Compounds (part 1-2)
Patai S. — The Chemistry of Organic Silicon Compounds (part 1-2)



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Название: The Chemistry of Organic Silicon Compounds (part 1-2)

Автор: Patai S.

Аннотация:

Organosilicon compounds are key organometallic compounds (R-Si) which have many uses in materials science and in metallurgy. Their applications include the synthesis of sugars and in the synthesis of organic compounds for the pharmaceutical industry. This volume will contain both updated chapters on key topics included in the original volumes as well as a number of new chapters reflecting the rapid developments made in silicon chemistry and its applications to organometallic chemistry, materials science, and semiconductors, over the last five years. As for the majority of volumes in this series, chapters will be prepared by leading scientists in the field.


Язык: en

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Год издания: 1989

Количество страниц: 1673

Добавлена в каталог: 16.04.2007

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID
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Предметный указатель
Tetrazoles, synthesis of      791
Teuben, J.H.M.      641 (246) 653
Teulade, M.P.      788 (107) 806
Textile treatment, siloxanes in      1349
Thames, S.F.      628 (200) 651 682 754 915 959
Than, K.A.      325 327 367 854 890 1417 1470
Thanedar, S.      1428 1462 1472
Thayer, J.S.M.      632 (219) 652 719 757 1144 1198 1199
The, K.I.      1255 1256 1286
Thenard, L.J.      18 (102f) 52
Theodorakoupoulos, G.      106 (148 149) 107 149) 109 149) 218
Theoretical aspects      57—213
Thermochemistry      371—389
Thermochemistry ionic species      446—454
Thermochemistry meaning of term      372
Thernard, L.J.      1242 (1) 1284
Thewalt, U.      (154) 275 302 1163 1203
Thiasilacyclopentanes, optically active      311
Thiel, W.      67 (53) 215
Thin-layer chromatography      433
Thio-substituted pentacoordinated silicon anions      206
Thioacylthiotriorganylsiianes      749
Thiophenes, silylated      685—686
Thiosilane      79 180
Thiosilanes analysis of      410
Thiosilanes properties of      1396
Thiosilanes reactions of      1396—1400
Thiosilanes synthesis of      1396
Thiosilylene      143
Thomas, A.P.      672 (90) 753 936 961
Thomas, D.B.      422 433 441
Thomas, D.R.      1299 1300 1357
Thomas, E.J.      953 (295) 962
Thomas, J.H.      722 (281) 757
Thomas, K.M.      234 235 236 295
Thomas, O.H.      911 (103) 958
Thomas, R.D.      270 (329) 301
Thomas, S.      1509 1510 1525
Thomas, T.H.M.      1323 (155 156) 1324 1325 156) 1326(155) 1327 156) 1328 156) 1329 1333 156) 1336 1341 156) 1359
Thome, A.J.      234 235 236 248 124) 249 124) 256 184) 295 297 298
Thompson, C.      203 (356) 224 814 820 821 835
Thompson, D.L.      176 (285) 222
Thompson, D.P.      999 (158) 1005 1130 1142
Thompson, D.W.      1248 (61) 1285
Thompson, E.      822 826 836
Thompson, H.W.      418 (283) 421 440 441
Thompson, J.      905 (62) 923 926 957 959
Thompson, J.C.      14 (98) 51 259 299
Thompson, J.F.      1120 (369) 1141 1406 1412
Thompson, M.E.      1444 (207) 1474
Thomson, C.      908 (70) 958
Thomson, J.B.      455 (54) 481 506 508 1011 1014
Thorli, E.Y.      721 (277) 757 888 892
Thorn, K.C.      1023 1031 1036 1039 1041 1043 1134
Thorn, K.L.      34 (181b) 54 1031 1135
Thrash, C.R.      427 (416) 432 442 444
Three-membered ring compounds      93—96
Three-membered ring compounds synthesis of      694—695
Thum, G.      1012 1013 1014 1429 1472
Thursock, R.A.      417 (266) 439
Tickle, P.      816 818 819 835 900 956
Tiemonium iodide, sila-analogue of      1172
Tierman, T.O.      486 (131) 508
Till, F.      425 (392) 426 431 454 459 460) 432 442 443
Till, L.      425 (392) 442
Tilley, T.D.      42 (224) 55 272 338) 275 301 302 1418 1420 1424 1425 82 83 85) 1426 86) 1432 1434 52) 1435 82 86 158) 1436 86) 1439 183) 1440 1444 1445 83 86) 1474 1448 1449 223) 1450 1453 1454 249) 1455 85 250—253) 1456 85 250 253 256—259) 1458 260) 1470 1471 1472 1473 1475 1476
Tillman, N.M.      1055 (192 193) 1056 1072 1074 1075 1137 1139
Timms, P.L.      421 422 360) 441
Timofeeva, T.V.      263 264 265 300
Timofeyeva, N.P.      1297 1299 1300 1357
Timoshenko, M.M.      617 620 650
Tin derivatives, PE ionization energies of      636 641
Tin, analytical determination of      398 401
Tinney, S.E.      797 (141) 807
Tirrell, M.      1315 (143) 1359
Tishenkov, A.A.      475 477 480 508 1127 1141
Titanium derivatives NMR data for      1440
Titanium derivatives PE ionization energies of      636 641
Titanium derivatives structural parameters of      272 274 1435
Titanium, analytical determination of      398 400 401
Tobin, M.C.      416 (229) 439
Tobita, H.      35 (188) 54 93 218 234 295 695 702 755 978 67 70) 980 982 1003 1019 28) 1020 1022 42) 1024 42) 1031 1036 1038 42 77) 1039 42) 1134 1135 1212 1238
Tochner, M.      429 (438) 443
Todesco, P.E.      790 (112) 807
Togo, H.      1397 (11) 1411
Tokach, S.      971 (28) 1002
Tokach, S.K.      967 (11) 1001 1051 168 170 172) 1086 168 170 172) 1137
Tokarev, M.I.      1091 1095 1096 1110 1114 1140 1407 1412
Toki, T.      1467 1470 1477 1519 1526
Tokuyama Soda Co.Ltd.      1151 (65) 1157 1158 1200 1202
Tokuyama, T.      1146 (38) 1200
Toler, J.R.      954 (307) 963
Tolls, E.      1374 (47) 1392
Tolstikov, G.A.      676 (108) 754 1497 101) 1523
Tomadze, A.V.      1120 (370 371) 1141
Tomao, K.      943 (245) 961
Tomas, M.      792 (122) 807
Tomasi, R.A.      948 (279) 962
Tominaga, K.      973 (44) 1002
Tominaga, Y.      1274 (143) 1280 1287 1288
Tomioka, H.      1157 (105) 1201
Tomita, A.      1509 (202b) 1526
Tomlinson, A.J.      1255 1256 1286
Tomoda, S.      943 (246) 961
Tong, C.C.      246 269 296
Top, S.      203 (355b) 224
Topchiev, A.V.      24 (133) 53 726 727 745 748 758 760 919 959 1482 32) 1483 1520 1521
Topiol, S.      84 86 217
Topsom, R.D.      896 (12) 902 42) 904 77) 956 957 958
Torgova, E.I.      426 (399) 442
Torn Dieck, H.      595 596 618 622 624 629 631 637 649 650
Torres, L.E.      802 (156) 807
Tossel, J.A.      129 130 220
Tossell, J.A.      84 86 217
Towart, R.      279 (390) 303 1149 50—52) 1164 1165 52) 1179 1200
Townes, C.H.      5 (31) 50
Towns, E.      1490 1491 1525
Townsend, L.B.      473 (96) 507
Toxicity, silatranes      1151
Toxicology      1183—1184
Toyoshima, S.      1157 (105—111) 1201 1202
Toyota, K.      1368 (24) 1369 29) 1391
Trachtman, M.      181 (296) 222
Tracy, V.M.      834 (145 146) 838
Traeger, J.C.      447 448 505
Traetteberg, M.      5 14 50 84 87 217 228 263 294
Traetteberg, T.      607 608 649
Trainor, J.T.      954 (304) 963
Trans-folding      234 235
Transannular alkoxy transfer      459
Transannular interaction      463
Transient species      469
Transition-metal catalysts, hydrosilylation using      1450 1458—1461 1480—1499 1500—1501
Transition-metal derivatives      1415—1469
Transition-metal derivatives alkene insertion into      1446—1449 1460
Transition-metal derivatives alkyne insertion into      1449—1450 1463 1464 1465
Transition-metal derivatives anions used      1419—1420
Transition-metal derivatives bonding in      1433—1435
Transition-metal derivatives carbon monoxide insertion into      1453—1458
Transition-metal derivatives catalytic reactions involving      1458—1470
Transition-metal derivatives coordinated Si-H bonds in      1437—1438
Transition-metal derivatives diene insertion into      1464
Transition-metal derivatives double-bonded derivatives      42
Transition-metal derivatives early transition-metal derivatives      1424—1427
Transition-metal derivatives electrophilic cleavage reactions of      1444
Transition-metal derivatives insertion reactions of      1446—1458
Transition-metal derivatives isocyanide insertion into      1455
Transition-metal derivatives late transition-metal derivatives      1417—1423
Transition-metal derivatives main-group metal silyls used      1420—1422 1424—1426
Transition-metal derivatives mass-spectrometry studies      1442
Transition-metal derivatives nitrile insertion into      1450
Transition-metal derivatives NMR studies      540—542 1438—1439 1440—1441
Transition-metal derivatives nucleophilic cleavage reactions of      1442—1444
Transition-metal derivatives organic carbonyl insertion into      1450—1453 1468
Transition-metal derivatives oxidative addition methods      1417—1419
Transition-metal derivatives PE ionization energies of      640—642
Transition-metal derivatives phosphorus-containing      1384—1387
Transition-metal derivatives reactions of      1442—1470
Transition-metal derivatives reductive elimination in      1444—1445
Transition-metal derivatives Si-H bond cleavage used      1426
Transition-metal derivatives stereochemistry of      322—328 356—358
Transition-metal derivatives structural parameters of      272—276 1433—1442
Transition-metal derivatives synthesis of      1416—1427 1429—1432
Transition-metal derivatives trans-influence of silyl ligand in      1437 1442
Transition-metal silene complexes      1432—1433
Transition-metal silicon clusters      1423—1424 1468
Transition-metal silylene complexes indirect evidence for      1427—1429
Transition-metal silylene complexes synthesis of      1429—1432 1463
Transition-metal silylene compounds      1423
Traylor, T.G.      617 (160) 650 897 18) 898 903 76) 956 958
Treadgold, R.C.      1144 (18) 1199
Trefonas III, P.T.      1226 (91) 1227 1229 1239
Trefonas, III, P.      1230 (109) 1230 1231 1240 1461 1476
Trefonas, P.      1234 (123) 1240
Tremelling, M.J.      726 (307) 758
Tremmel, J.      232 (40) 295 563 647
Trenerry, V.C.      449 (33a 33c) 487 488 139) 489 143) 490 493 497—500 506 509
Trepka, W.J.      699 (188) 755
Treverton, J.A.      374 376 378 381 47) 382 383 390
Tri-t-butoxysilanthiolates      268
Triazidophenylsilane PE spectrum of      568 569
Triazidophenylsilane synthesis of      720
Triazoles silylated      689
Triazoles synthesis of      791
Tribble, M.T.      68 101 215
Trickle, I.R.      568 570 647
Tricyclamol iodide, sila-analogue of      1172 1174
Tridihexethyl chloride, sila-analogue of      1172
Triethylsilane      802
Triethylsilane reduction by      777 778
Triethylsilylhydrotrioxide      802
Trifluorosilyl radical      199
Triggle, A.M.      279 (391) 303
Triggle, D.J.      279 (391) 303
Trigonal-bipyramidal complexes, stereochemistry of      364—365
Trigonal-bipyramidal geometry      281 282 1249 1250
Trigonal-bipyramidal geometry axial entry in      1254
Trigonal-pyramidal complexes, site preferences in      1251—1257
Trigonopsis variabilis (DSM 70714)      1194 1195 1196
Trihydroxysilane      83
Trimercaptosilane      83
Trimethyisilyi triflate      726 729 773—776 803
Trimethyl-n-pentyloxysilane ions      455—456
Trimethylazidosilane      719
Trimethylbromosilane      765
Trimethylchlorosilane      764—765
Trimethylenemethane palladium complexes      782—783
Trimethyliodosiiane      765 766—768 788
Trimethylmethoxysilane      783
Trimethylphenylsilanes metabolic fate of      1186
Trimethylphenylsilanes synthesis of      681 682
Trimethylsilane, photolysis of      967
Trimethylsilanol, synthesis of      723
Trimethylsilyi-nitrile oxide, isoxazoles synthesized using      691
Trimethylsilyl anion      494
Trimethylsilyl azide      795—796
Trimethylsilyl carbocations, NMR spectra of      519
Trimethylsilyl cation      448—449 455
Trimethylsilyl cyanide      768—773 777
Trimethylsilyl methyllithium      787
Trimethylsilyl methylmagnesium bromide      789
Trimethylsilyl nitrate      688
Trimethylsilyl radical      199
Trimethylsilyl-1, 3-butadiyne      785
Trimethylsilylbenzocyclopropane      674—675
Trimethylsilyldiazirine, formation during photolysis      989
Trimethylsilyldiazomethane, photolysis of      989
Trimethylsilylethynyllithium      785
Trimethylsilylethynylmagnesium bromide      786
Trimethylsilyllithium      269—270 271
Trimethylsilylmethyl group, as donor substituent      576—577
Trimethylsilylmethylene, formation during photolysis      989
Trimethylsilylphenols, acidity of      817
Trimethylsilylpyridines quinolizines synthesized using      693
Trimethylsilylpyridines synthesis of      692
Trimethylsilyltriazoles      689 790
Trimethyltriphenyldisilane      45
Trinberg, L.      352 353 369
Trindle, C.      946 (269) 962
Trinquier, G.      13 15 16 51 60 101 102 103 106 107 114 125 157) 126 128 129 130 133 136 150 185 213 218 219 1046 1050 1054 1079 1085 161) 1086 1089 1090 1136 1137
Triorganylsilanes, stability of      707
Triparanol, sila-analogue of      1178—1179
Triphenylchlorosilane, kinetics of reaction      852
Triphenylsilyl azide, photolysis of      993
Triphenylsilyl perchlorate, structure of      1012
Triphosphasilacyclobutane      1381
Triphosphines, silyl-substituted      1375
Triplett, K.      47 (272a) 56
Triply bonded silicon compounds      145—151 1131—1133
Triply coordinated silicon compounds, PE spectra of      560—563
Tripodi, M.K.      447 (19a) 505
Trippett, S.      1256 (102) 1286
Tris(benzene-1, 2-diolato) complexes, reactivity of      1271—1273
Tris(trimethylsilyl)arsines      1388
Tris(trimethylsilyl)bismuthines      1390
Tris(trimethylsilyl)heptaphosphanotricyclene      635 1384
Tris(trimethylsilyl)ketimine      711
Tris(trimethylsilyl)methyl derivatives bimolecular substitution reactions of      884—885
Tris(trimethylsilyl)methyl derivatives nucleophile-induced fragmentation of      886—887
Tris(trimethylsilyl)methyl derivatives reactions of      880—882
Tris(trimethylsilyl)methyl derivatives rearrangement of      881 888
Tris(trimethylsilyl)methyl derivatives solvolysis of      885—886
Tris(trimethylsilyl)methyl ligand      880
Tris(trimethylsilyl)methylbenzene, photolysis of      968
Tris(trimethylsilyl)phosphine      1366 1369 1384
Tris(trimethylsilyl)stibines      1389
Tris-chelate dianions      1247
Trisilabicyclo[1.1.0] butanes      101
Trisilacyclopropane      172
Trisilane      84 88
Trisilanes, photolysis of      977 978—979
Trisilthianes      1404
Trisilylphosphines      1377
Trisyl, meaning of term      880 1010
Trithiosilane      83
Trivalent silyl ions      1007—1013
Trofimov, B.A.      1485 (48) 1521
Tropolonate derivatives, protonolysis of      1267
Tropolonate derivatives, protonolysis of ropones cycloaddition reactions      784
Tropolonate derivatives, protonolysis of ropones trimethylsilyl cyanide added to      769
Trost, B.M.      740 (388) 760 783 784 786 796 806 807 924 960
Troung, P.W.      103 104 105 106 107 109 111 129 131 132 133 137 138 140 143 218
Troung, T.N.      119 (181) 129 130 131 133 134 135 137 138 213a) 139 150 151 177 178 199) 179 199) 203 219 220
Truesdale, L.K.      1398 (16) 1411
Truong, P.N.      586 (112) 648
Truong, T.N.      11 (63) 51 260 261 299 1028 1134
Tsai, D.J.S.      949 (287) 962
Tsai, R.S.C.      467 481 482 507 508
Tsai, Y.M.      940 (228) 961
Tsang, W.      384 (56) 390
Tsapenko, V.R.      1151 (60 61) 1152 61) 1200
Tsarenko, A.F.      1336 1337 1360
Tsay, Y.H.      233 (42) 270 295 301
Tschmutowa, G.      556 558 559 615 638 644 645 652
Tse, F.L.S.      1154 1155 1188 1201
Tse, J.S.      579 587 589 591 592 593 604 613 617 618 619 648 649
Tseng, D.      972 (34) 1002
Tsetlina, E.O.      749 (436) 761 1484 1521
Tsipis, C.A.      275 (378) 302 662 752 1484 44b 45) 1521
Tsitsishvili, G.V.      1493 (83) 1522
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