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Rappoport Z. (ed.) — The Chemistry of Dines and Polyenes (vol. 1)
Rappoport Z. (ed.) — The Chemistry of Dines and Polyenes (vol. 1)



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Название: The Chemistry of Dines and Polyenes (vol. 1)

Автор: Rappoport Z. (ed.)

Аннотация:

Dienes and polyenes are an extremely important group of chemicals in the investigation of different types of syntheses. Dienes and Polyenes are found in a large number of natural and man-made products including such natural products as terpenes, cholesterol, Vitamin A, and many essential oils, as well as many polymers and rubber products. In recent years the organometallic complexes of these compounds have been found to play an important role in synthesis. This volume is an invaluable reference source for researchers in academia and industry in organic and natural product chemistry and materials science. An extensive work covering all aspects of the synthetic analytical, biochemical, physical, and environmental aspects of these important molecules.


Язык: en

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Год издания: 1997

Количество страниц: 1054

Добавлена в каталог: 20.04.2006

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID
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Предметный указатель
Dehydrotosylation, as synthetic procedure for conjugated dienes      368 369
Deiters, U.      559 561 563(52) 613
Dejroongraung, K.      71(llb) 72(llb 14) 77 88(11b) 104 105
deKock, R.J.      268(16a) 320
Del Bene, J.      242(292) 261
Delhalle, J.      2 15(2) 20
Dellepiane, G.      166(115) 172
Delton, M.H.      402(135) 472
DeLucca, G.      45(110) 64 181 185(98) 256
DeLucchi, O.      277(32c) 321
Delugeard, Y.      53(154) 65
Dembek, A.A.      155(37) 170
Demuth, M.      281(41b) 321
Denis, J.-M.      881(36) 886 945(40) 975
Denissen, J.F.      848(194) 866
Denmark, S.E.      455(282a) 479 509(9a 9b) 544
Density fractional theory      3 18
Deoxygenation, reductive, as synthetic procedure for conjugated dienes/polyenes      368—372
Dep, B.      463(303a) 480
Depezay, J.C.      412 414(162c) 473 782(23) 861
DePuy, C.H.      735(8 10) 736(13) 738 739(8) 750
Derguini, F.      141(50b) 147
Derone, A.E.      606(185b) 617
Desai, S.R.      398(118) 471
Descoins, C      454 455(278a) 479
DeShong, P.      417(164c) 473
Desmaele, D.      301(85a 86) 323
Desmond, R.      533(101) 546
Desrosiers, M.      337(45) 355
Dessau, R.M.      631 632(53) 645(53 87) 651 652
Desulphonylation, reductive, as synthetic procedure for conjugated dienes      375 376
Dettmer, G.      535(106) 546
Deuter, J.      44(102—104) 64
Dev, S.      276(30a) 320 453(276b) 479
Devaux, P.      500(43) 505
DeVita, RJ.      666(42) 680
DeVoe, H.      133(41a) 147
Devyatykh, G.G.      802(67) 862
Dewar benzene, structure of      43
Dewar pyrones      268 270
Dewar, M.J.S.      2 17(5) 20 32(23) 62 102(99b) 110 207(178) 225(212) 258 259 630(48) 651
DeWitt, E.J.      717(58) 732
Dfflet, V.      17 19 20(129) 23
Dhanoa, D.S.      627 631 633—635(39) 650
Di-$\pi$-methane rearrangements      277—280 (see also “Aza-di-$\pi$-methane rearrangements”)
Diacyloxylation      662 663
Diacyloxylation aerobic      667 668
Dickerson, J.E.      434(209d) 435(218) 476
DiCorato, A.      117 135(12) 146
Dicyanomethyl radical, addition to dienes      621 622
Diechsel-Grau, E.      621 622(11) 650
Dieck, H.A.      438(228) 477
Diederich, F.      56(167) 65 940 945(26a) 971 973(107 108) 975 977
Diederichs, F.      58(180) 65
Diedrich, M.K.      599(163) 602(174) 603(190) 606(186) 607(187) 608(188) 616 617
Dieleman, J.      228 232(215) 259
Diels — Alder reactions      (see also “Retro — Diels — Alder reactions”)
Diels — Alder reactions, catalysis of      19 20
Diels — Alder reactions, diastereofacial selectivity in      19
Diels — Alder reactions, effect of pressure on      552—596 603—607
Diels — Alder reactions, effect of pressure on mechanistic aspects of      552—563
Diels — Alder reactions, effect of pressure on synthetic applications of      563—591
Diels — Alder reactions, intramolecular      511—518 603—607
Diels — Alder reactions, mechanism of      17—19
Diels — Alder reactions, mechanism of, isotope effect studies of      776 848—854
Diels — Alder reactions, pincer/domino      573 575
Diels — Alder reactions, regioselectivity in      19
Diels — Alder reactions, site-selectivity in      19
Diels — Alder reactions, solvent effects on      19 20
Diels — Alder reactions, stereoselectivity in      19
Diene chirality rule      117—120 131
Diene rule      139
Dienes      (see also ”Bis-dienes” “Butadienes” “Decadienes” “1 “1 “Heptadienes” “Hexadienes” “Norbornadienes” “Norcaradienes” “Octa-dienes” “Pentadienes” “Propelladienes” “Spirodienes”
Dienes cisoid      112 113 120—122 126
Dienes distorted      114 117 118 126—132
Dienes transoid      112 113 131
Dienes, electronic spectra of      236
Dienes, PE spectra of      178—182
Dienes, polymerization of, radiation-induced      343—346
Dienes, radiolysis of in aqueous solntion      327—334
Dienes, radiolysis of in non-aqueous solvents      334—339
Dienes, reactions of, with hydrated electrons      328
Dienes, reactions of, with hydrogen atoms      328
Dienes, reactions of, with hydroxyl radicals      328
Dienes, s-cis      6 7 112—114 126 128—134 141 142
Dienes, s-trans      41 112—114 117 135—137 141 142
Dienes, skewed      131 132
Dienes, synthesis of, $\sidset{^{125}}{}I$-labelled      844—846
Dienes, synthesis of, $\sidset{^{14}}{}C$-labelled      827 828 831 832 841—843
Dienes, synthesis of, deuterium-labelled      776—802
Dienes, synthesis of, tritium-labelled      818—822
Dienoates      see “Eicosadienoates”
Dienones      see “Cross-conjugated dienones” “Cycloalkadienones”
Dienophiles, unsymmetrical, in Diels — Alder reaction      18 19
Dienth, W.      34(41) 62
Dienyl radical cations      338
Diercksen, G.H.F.      211(189) 258
Diessel, J.      181; 184 185(92) 256 365(23c 23d) 468
Dietrich, H.      56 57 61(166) 65
Dietz, F.      974(110) 977
Dieue chromophore, $C_2$      120
Dieue chromophore, distortion of      114 117 118
Dieue chromophore, electronic absorption spectrum of      112—114
Dihydrocostunolide, synthesis of      272
Dihydronaphthalenes, structure of      45
Dihydronaphthalenes, thermochemistry of      90 99
Dihydronaphthalenes, [4+4]photocycloaddition of      306 307
Dihydronovanin, synthesis of      272 273
Dihydropyrans, synthesis of      268 270
Diing, L.G.      818(102) 863
Diisko, R.L.      26(1) 61
Dill, J.D.      184(144) 257
Dilworth, B.M.      374(52f) 469
Dimichele, L.      440 441(244c) 477
Dimitrova, BA.      485(9) 504
Ding, R.S.      338(59 60) 355
Ding, S.F.      822(116) 864
Dinne, E.      510(13) 544
Diols, formation of      891
Diols, unsaturated, reductive deoxygenation of      368—372
Dioxythiepines, photocycloaddition of      315 318
Diphenylallyl anions      747 748
Diphenylphosphonyl radicals, addition to dienes      623
Dirac, P.A.M.      152(21) 170
Dirkzwager, H.      770(22) 774
Dispirodecadiene, structure of      42
Ditchfield, R.      78(27) 106
Dittami, J.P.      280(39) 321
Divinyl ketones, cyclization of      508 509
Dixon, D.A.      15(86) 22
Djerassi, C      485 489 490 496(7) 504
Djuric, S.W.      440 441(244a) 477
Do, U.H.      860(238) 867
Dobler, W.      185(165) 258
Docosahexaenoates, deuterium-labelled, synthesis of      780 781
Docosahexaenoic acid, $\sidset{^{11}}{}C$-labelled, synthesis of      824 825
Dodecahedranes      50
Dodelet, J.P.      335(25) 339(73) 354 355
Doecke, C.W.      181(94) 256
Doering, J.P.      11(64 65) 22
Doering, W.V.E.      39(79) 54(158) 63 65 76 77(23) 78(26) 98(23) 106 179(37) 183 184(117) 211(37) 255 257 559(51) 596(158) 608(189) 613 616 617 627(25 27) 650
Dogan, B.      80(32) 98(82) 106 109 570 573(86) 614
Dogan, B.M.J.      559(51) 560(53) 562(59) 570 573(87) 574(91) 595 596(152) (153) 613 614 616
Dolbier, W.R.      594 595(149) 616
Dolbier, W.RJr.      76 77(23) 78(26) 98(23) 102(100) 106 110 858(231 232) 859(232) 866
Dole, M.      347(109) 351(139 140) 356 357
Dolle, R.E.      410(155c) 415 422(171e) 473 474
Dolman, D.      277(33) 321
Domaille, P.J.      52 53(144) 65
Domalski, E.S.      70(9) 104
Domcke.W.      211(189) 258
Domelsmith, L.N.      181(84) 225(213) 256 259
Domingues, E.      438 439(234a) 477
Domnin, I.N.      179(41) 255
Domow, R.      621 622(11) 650
Doney, J.J.      424 425(179c 179d) 475
Doning, D.      440 442(244e) 477
Donkersloot, M.C.A.      119(19a 19c) 146 147
Doolittle, R.E.      455(282b) 479
Dore, L.      53 54(159) 65
Dorfman, L.M.      327(9) 354
Dorko, E.A.      56(164 165a 165c) 57 58 61(164) 65 931(2) 974
Dosio, F.      823(122) 864
Dowbenko, R.      522(62) 545
Doxsee, K.M.      427(185) 475
Doyle, A.M.      717(56) 732
Dragonette, K.S.      33(34) 62
Drake, A.F.      116 117 132 133(10) 146
Drake, S.R.      791(42) 862
Dreiding, A.      43(97) 63
Drew, M.B.G.      586(114) 615
Dromzee, Y.      376(61) 469
Drouin, J.      181 184(97) 256
Drummond, G.S.      847(192) 866
Dube, D.      388 390(96d) 470
Dubois, J.-E.      631 632 643 649(54b) 651
Dubuis, R.      453(276a) 479
Dudis, D.      15(85) 22
Dudis, D.S.      15(80) 22
Dudley, G.K.      344(94) 356
Duhamel, L.      382(83f-h 84—86) 384(83f-h) 418(86) 419(83f) 470
Duhamel, P.      382(83f 83g 86) 384(83f 83g) 418(86) 419(83f) 470
Duke, AJ.      401(132b) 472
Dumer, G.      266(10a 10b) 319
Dunbar, R.      229(218—220) 230(219 220) 236(237 238) 249(238) 259 260
Dunbar, R.C.      179(25) 184(149) 236(244 245 252 267 272) 237(281) 248(267) 249(245 252) 255 257 260 261
Duncan, J.H.      377 378(69a) 469
Dunitz, J.D.      37(57) 58 60(181) 63 65 964(97) 976
Dunkin, I.R.      236(263) 237(263 285) 248(285) 249(263 285) 260 261
Dunogues, J.      673(57c) 681
Dunston, J.M.      289(55b) 322
Duplantier, AJ.      420(166c) 474
Dupont, G.      141(52a) 147
Dupous, M.      4(12 17) 21
Dupuis, M.      15(79) 22 31(15—17) 35(17) 61 166(109) 172
Duraisamy, M.      136(44a 44b) 147
Duran, M.      16(93) 17 19 20(123) 22 23
Durig, J.R.      6(41) 21
Durst, T.      404(137c) 472 610(201) 617
Duthaler, R.      298(77b) 322
Dykstra, C.E.      16(92) 22
Dynamic coupling      123 133
Dyomin, P.M.      813(98) 863
Dzhemilev, U.M.      907(102) 924
D’Aloisio, R.      912(138) 925
d’Angelo, J.      17 19 20(108) 22
E-$\sidset{^{125}}{}IVNNT$, synthesis of      844 845
Easwaran, K.R.K.      141(51a) 147
Eaton, D.F.      179(30) 255
Eberbach, W.      181(87) 256
Eberhardt, A.      34(42) 62 440 443(245c) 477
Ebrey, T.G.      141(50a) 147
Ebsworth, E.A.V.      179(43) 255
Echegoyen, L.      772(24) 774
Echinocandin B, $\sidset{^2}{}H$- and $\sidset{^3}{}H$-labelled, synthesis of      801 802
Echter, T.      958(79) 976
Eckell, A.      274(26) 320
Eckert, CA.      554(34) 556(39) 557(40 41) 558(47a 47b) 612
Eckert-Maksic, M.      26(5) 61 177(12) 180(12 65) 181(65) 221(208) 254 255 259
Eckrich, T.M.      439(239 240a) 477
Edenborough, M.S.      606(185b) 617
Edge effects, in long polyenes      10
Edmiston, C      220(205) 259
Edmunds, J.E.      440(248) 478
Edwards, J.M.      126 134(36) 147
Edwards, M.P.      388 389(96a) 470
Edwards, P.D.      894(22) 922
Efimov, I.B.      352(142) 357
Eftenberger, F.      411(155f) 473
Egawa, Y.      232(228) 259
EgHnton, G.      493(18) 504
Egmond, M.R.      917(172) 925
Ehrenson, S.      688(16) 731
Eichel, W.      621 622(11) 650
Eicher, T.      379(76a) 470
Eickhoft, D.J.      907(113) 924
Eicosadienoates, deuterium-labelled, synthesis of      778
Eicosatetraenoic acids, $\sidset{^{11}}{}C$-labelled, synthesis of      825 826
Eicosatrienoates, deuterium-labelled, synthesis of      778—780
Eisenstein, O.      17 19 20(116) 23
Eiter, K.      364(24b) 468
Ejiri, E.      428 429(190e 190f) 475
El Tayar, N.      802(64) 862
El-Dim, G.N.      609(193) 617
El-Din, G.N.      588(122) 610(200) 615 617
El-Sayed, MA.      150 151(10) 170 183(119) 257
Eland, J.H.D.      175(9) 179 184(18) 254
Elango, V.      417(164c) 473
Eldik, R.van      548(4 6) 611
Electrical effects      687—702
Electrical effects, classification of      690 692—698
Electrical effects, parameters for      698—702 728 729
Electrical properties, molecular      15 16
Electrocyclic reactions      507—510
Electrocyclic reactions photochemical      265—276
Electrocyclic reactions, effect of pressure on      597 599 602
Electron affinity      733 734
Electron capture detection      500
Electron correlation      3
Electron energy loss spectroscopy, in structure determination of dienes      486 488
Electron nuclear double resonance spectroscopy      499
Electron spin resonance spectroscopy of oligomer radicals      344
Electron spin resonance spectroscopy of polymers      349
Electron spin resonance spectroscopy of radiolytic radical cations      337 338
Electron-electron interactions      214
Electronic spectroscopy      228—239
Electronic spectroscopy of dienes      236
Electronic spectroscopy of polyenes      236—238
Electronic transitions      11
Electrophilic aromatic substitution, intramolecular      291 292
Elix, JA.      366(27) 468
Eller, B.C.      845(182) 865
Ellerman, T.      339(67) 355
Ellis, D.E.      871(15) 886
Ellison, G.B.      11(61) 22 735 738 739(8) 750
Ellsworth, R.L.      840(172) 843(176) 865
Elsasser, D.      182(110 113) 257
Elvidge, JA.      822(115) 864
El’yanov, B.S.      552(30) 592(141) 598(162) 612 615 616
Ema, K.      350(133 134) 357
Emken, E.A.      778(6 9) 861
Emram, J.      855 857(225) 866
Enantiodivergent synthesis      663
Enchev, V.      51(138) 64
Enders, D.      387(94) 470
Endo, Y.      51(130) 64
Endoperoxides, formation of      891
Ene reactions, intramolecular      518—521
Ene reactions, metallo      520
Ene-allenes, cyclization of      541 542
Eng, W.      809 810(87a 87b) 863
Engberts, J.B.F.N.      591(133) 615
Engelhardt, L.M.      182(109) 257
England, W.      220(205) 259
Englert, G.      493(19) 504(54) 505
English, J.H.      236(269) 260
Engman, L.      366 367(28d) 468
Enkelman, V.      34(42) 62
Enkelmann, V.      440 443(245c) 477
Enoki, T.      963(89) 976
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