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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

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Предметный указатель
Conjugated dienes, oxidation of, with metalloporphyrins      899
Conjugated dienes, oxidation of, with osmium tetraoxide      897 898
Conjugated dienes, oxidation of, with ozone      920
Conjugated dienes, oxidation of, with permanganate      892 893
Conjugated dienes, oxidation of, with peroxo compounds      903—905 907 908 911 912
Conjugated dienes, oxidation of, with singlet oxygen      914 915
Conjugated dienes, oxidation of, with triplet oxygen      917—919
Conjugated dienes, Paterno — Buechi reactions of      297—306
Conjugated dienes, photodimerization of      296 297
Conjugated dienes, photoenolization of      264 265
Conjugated dienes, radical addition to      620—627
Conjugated dienes, regioselectivity of      630—634
Conjugated dienes, structure of      31—37
Conjugated dienes, synthesis of, by addition-elimination reactions      378—395
Conjugated dienes, synthesis of, by carbene insertion reactions      465
Conjugated dienes, synthesis of, by concerted reactions      395—406
Conjugated dienes, synthesis of, by coupling reactions      427—442 444—453
Conjugated dienes, synthesis of, by elimination reactions      364—378
Conjugated dienes, synthesis of, by Vilsmeier reaction      464
Conjugated dienes, synthesis of, by Wittig and related reactions      407—409 412—417 420—422 424—427
Conjugated dienes, synthesis of, from aikynes      453—457
Conjugated dienes, synthesis of, from allenes      466 467
Conjugated dienes, synthesis of, from arenes      465 466
Conjugated dienes, synthesis of, from cyclopropanes      465
Conjugated dienes, synthesis of, from heterocycles      457—462
Conjugated dienes, synthesis of, from oxoketene dithioacetals      463
Conjugated dienes, thermochemistry of      75—79
Conjugated dienes, [4+4]photocycloaddition of      306—313
Conjugated polyenes, cyclization of      507 510
Conjugated polyenes, linear, electronic structure of      243—250
Conjugated polyenes, planar, deviations from planarity in      209—211
Conjugated polyenes, planar, electronic structure of radical cations of      199—215
Conjugated polyenes, structure of      31 32 34—36
Conjugated polyenes, synthesis of, by addition-elimination reactions      379—388 392 394 396
Conjugated polyenes, synthesis of, by concerted reactions      397 405
Conjugated polyenes, synthesis of, by coupling reactions      428—431 434—438 440 443—445 447—449 451 452
Conjugated polyenes, synthesis of, by elimination reactions      366 369—374 377
Conjugated polyenes, synthesis of, by Wittig and related reactions      410 411 413 414 418—425
Conjugated polyenes, synthesis of, from aikynes      453—455
Conjugated polyenes, synthesis of, from heterocycles      457—462
Conjugated polyenes, synthesis of, from oxoketene dithioacetals      463 464
Conjugated polyenes, synthesis of, from tropone oxime tosylate      464
Conjugated polyenes, thermochemistry of      87—91
Conjugation energy      76 77
Conjugation, in determination of stable conformations      7
Conlon, L.E.      854 855(213) 866
Conolly, J.W.      639(74 75) 651
Conover, W.W.      921(214) 926
Conrad, N.D.      857(230) 866
Contelles, J.L.M.      366 367(28a) 468
Contreras, B.      382(85) 470
Cook, B.R.      899(57) 923
Cook, R.L.      39(76) 63
Cooke, DA.      483 484 493(6) 504
Cooke, RJ.      897(43) 923
Cookson, R.C.      276(30d) 320
Cooney, M.J.      963(90b) 976
Cooper, D.M.      905(92) 924
Cooper, J.L.      526(75) 545
Cooper, M.      844(179) 865
Cope rearrangement      28 48 49 510 511
Cope rearrangement effect of pressure on      596—599
Copenhafer, R.A.      311(106c) 323
Copolymerization      346 351
Corcoran, J.W.      420(166a) 474
Corey, E.J.      268(14c) 272(19a 19b) 313(14c) 320 372(47a) 385(88) 387(94) 416(164a) 439(239 240a) 440(247) 469 470 473 477 631(60) 633 640(62) 645(60 88) 651 652 810(89) 863 898(49) 923
Corma, A.      911(132) 925
Corman, M.L.      847(189) 866
Coronene, structure of      41
Correia, C.R.D.      296 306(72) 322
Correlation techniques      222—224
Cosstick, K.      561(63c) 613
Costa, M.      466(313e) 480
Costain, C.C.      498(40) 505
Cottard, M.      416(164b) 434(209c) 473 476
Coulomb integrals      228
Coulson, CA.      209(182) 258
Coupled cluster (CC) method      3
Coupled oscillator model      120 133
Cowan, D.O.      26(1) 61 942(35a) 975
Cox, N.J.G.      629(46) 651
CR equation      689
Cradock, S.      179(43) 233(231) 255 260
Cragoe, EJJr.      827(144) 864
Craig, D.      511(23) 544 720(62) 732
Craig, R.H.      847(191) 866
Craig, W.G.      892(2) 922
Cram, D.J.      739(26) 750
Crandall, J.J.      921(214 215) 926
Crandall, J.K.      179 180 211(17) 254 265(6) 285(51) 319 321 529(87b 87c 88) 545 905(90—93) 924
Cravotto, G.      409(154d) 473
Crawford, J.      406(148) 472
Cremer, D.      31(19) 51(137c) 61 64
Cresp, T.M.      570(89) 614
Crews, P.O.      39(78) 63
Crich, D.      626(20) 650 824(124) 864
Criegee, R.      895(25 26) 896(26) 921(208 210) 923 926
Crimmins, M.T.      264(3a) 319
Crisp, G.T.      509(10) 544
Crispino, G.A.      897(44 46) 923
Crist, B.V.      119 124 125(26) 129(38) 130 134(38 39) 147
Cristeau, H.J.      788(37) 862
Crocetins, formation of      265 266
Cromack, K.R.      337(42) 355
Crombie, L.      459(296) 479
Crooks, E.L.      71 72 77(11a 11b) 78(26) 88(11a 11b) 104 106
Cross-conjugated dienes, electrosynthesis of      773
Cross-conjugated dienones, photorearrangement of      280—295
Cross-conjugated polyenes, radical cations of      250
Cross-conjugation      52 53 57 93 94 98 928—930
Cross-linking      347 348 351
Crossley, M.J.      894(19) 922
Croteau, R.      819(108) 859(236) 863 867
Crotonolactone, Diels — Alder reaction of      19
Crouch, R.D.      406(149) 472
Crouse, G.D.      841(173) 865
Crousse, B.      438 439(233) 455(283a) 477 479
Crowley, KJ.      265(6) 274(25) 319 320
Cruse, W.B.      415(168c) 474
Cruz, PJ.D.      845(180) 865
Crystallization, in situ, of bridged polyenes      46
Csaszar, P.      162 164(87) 171
Cserep, Gy.      339(72) 340(84) 341(77 79) 355 356
Csoregh, I.      658(23) 680
Cui, C.X.      4(17) 21 166(120) 172
Cuisiat, S.V.      315(112a) 324
Cullen, D.L.      43(97) 63
Cumulated dienes      68 (see also “Allenes”)
Cumulated dienes, thermochemistry of      73
Cumulated dienes, [2+2]cycloadditions of      591 593—595
Cumulated polyenes, thermochemistry of      73—75
Cunard, N.      306(90a) 323
Cunningham, A.F.Jr.      465(309b) 480
Curran, D.P.      522(60) 545 620(2) 628(44) 633(63) 650 651
Curry, B.      150 169(11) 170
Cuthbertson, G.R.      98(81) 109
Cutting, J.D.      907(107) 924
Cuvigny, T.      375(59) 469
Cvetanovic, R.V.      631(50) 651
Cybulski, S.M.      738(23) 750
Cyclic dienes      (see also “Bicyclic dienes” “Cycloalkadienes” “Polycyclic
Cyclic dienes, mass spectra of      489—492
Cyclic dienes, ring opening of, photochemical      265—268
Cyclic dienes, structure of      37^-0
Cyclic dienes, thermochemistry of      80—85
Cyclic polyenes      (see also “Bicyclic polyenes” “Cycloalkatetraenes” “Cycloalkatrienes” “Polycyclic
Cyclic polyenes metal-complexed, photocycloaddition of      315—318
Cyclic polyenes, structure of      37 38 40 41
Cyclization reactions      (see also “Cope rearrangement” “Diels “Electrocyclic “Ene “Macrocyclization “Spirocyclization
Cyclization reactions anionic      536—539
Cyclization reactions cationic      525—536
Cyclization reactions free-radical      522—525
Cyclization reactions isotope effects in      859
Cyclization reactions metal-catalysed      539—542
Cycloaddition reactions, isotope effects in      858 859
Cycloaddition reactions, photochemical      279 293 295 306—318
Cycloalkadienes      see “Cyclic dienes” “Cycloheptadienes” “Cyclohexadienes” “Cyclooctadienes” “Cyclopentadienes”
Cycloalkadienones      see “2 “2 “2
Cycloalkanes      see “Alkylidenecycloalkanes” “Cyclohexanes” “Cyclopropanes”
Cycloalkatetraenes      (see also “Cyclooctatetraene”)
Cycloalkatetraenes, structure of      40
Cycloalkatrienes      (see also “Cycloheptatrienes” “Cyclooctatrienes”)
Cycloalkatrienes as rearrangement products      43
Cycloalkenes      (see also “Alkylidene-cycloalkenes” “Cyclobutenes” “Cyclo-heptenes” “Cyclohexenes” “Cyclopropenes”
Cycloalkenes, kinetic acidities of      748
Cyclobutenes      (see also “3
Cyclobutenes, formation of      508
Cyclobutenes, ring opening of      402—405
Cycloheptadienes, radiolysis of      337
Cycloheptadienes, thermochemistry of      82
Cycloheptadienes, tritium-labelled, synthesis of      821 822
Cycloheptatrienes      (see also “Methylene-cycloheptatrienes”)
Cycloheptatrienes, Diels — Alder reaction of      568 571
Cycloheptatrienes, radical reactions of      328
Cycloheptatrienes, radiolysis of      337
Cycloheptatrienes, tritium-labelled, synthesis of      821 822
Cycloheptenes      see “Bicyclo[3 2 0]heptenes”
Cycloheptenols      see “Vinylbicycloheptenols”
Cyclohexadienes      (see also “1 “1 “Methylenecyclohexadienes”
Cyclohexadienes radiolysis of in aqueous solution      328—334
Cyclohexadienes radiolysis of in non-aqueous solvents      335
Cyclohexadienes radiolysis of, gas-phase      341 342
Cyclohexadienes, thermochemistry of      81 82
Cyclohexadienyl radicals      330 341
Cyclohexadienyl radicals, dimerization of      331
Cyclohexadienylperoxyl radicals      332
Cyclohexanes      see “1 “Hexakis(ethylidene)cyclohexane”
Cyclohexenes      see “Bicyclo[3 4-Hydroxycyclohexene”
Cyclohexenyl radicals      341
Cyclooctadienes      (see also “Bicyclooctadienes” “1 “1
Cyclooctadienes thermochemistry of      82 83
Cyclooctanoids, synthesis of      311
Cyclooctatetraene      100 101
Cyclooctatrienes      (see also “Benzocyclooctatrienes” “Bromocyclooctatriene”
Cyclooctatrienes, thermochemistry of      89 90
Cyclopentadienes      (see also “Methylenecyclopentadienes”)
Cyclopentadienes, Diels — Alder reaction of      20
Cyclopentadienes, Paterno — Buechi cycloaddition of      298 299
Cyclopentadienes, thermochemistry of      80 81
Cyclopentadienyl anions      734
Cyclopentenones, synthesis of      282 290 291
Cyclopropanes      (see also “Spirocyclopropanes” “Tris(2-adamantylidene)cyclopropane” “Tris(fluoren-9-ylidene)cyclopropane” “Tris(quino)cyclopropane” “Vinylcyclopropanes”)
Cyclopropanes, ring opening of      466
Cyclopropenes      see “Methylenecyclopropenes”
Cyclopropyl-conjugation      41 42 49
Cytoprotective activity, determination of mechanism of      776
Cyvin, S.J.      33(31) 62 161(80) 171
Cywar, D.A.      623 624(15 16a) 650
Dabestani, R.      308(101c) 323
Dactylol, synthesis of      313 314
Daeuble, J.F.      514(36) 544
Dagdagan, O.A.      70 71 88(7) 104
Dahlen, S.E.      783(24) 862
Dahlke, G.D.      740(37) 750
Dahmen, A.      510(14) 544
Dai, S.      236(259 260) 250(260) 260
Dai, S.H.      858(231 232) 859(232) 866
Dailey, W.P.      276(30b) 320
Daines, R.A.      420(166c) 423(172c) 474
Daintith, J.      210 211(185) 258
Daka, M.R.      597 600(169) 616
Dalh, A.R.      777(2) 778(4 5) 861
Dallinga, G.      38(62 64) 63
Dallinger, R.F.      338(65) 355
Dalton, J.C.      297(75) 298(77a) 322
Daluge, S.M.      847(191) 866
Damiani, D.      38(60) 53 54(159) 63 65
Damodaran, K.M.      844 845(177) 865
Damodaran, N.P.      276(30a) 320
Damrauer, R.      736(13) 750
Dana, G.      642(83) 652
Dang, H.P.      438(229) 477
Daniel, D.S.      119(17) 146 273(22) 320
Daniels, K.      907(113) 924
DaniewsK, W.M.      590(128) 615
Danilova, N.A.      431(198b) 476
Danishefsky, S.      565(79) 613 895(33) 923
Danjo, H.      818(107) 863
Dannacher, J.      179(22) 236(268) 255 260
Dannenberg, I.J.      17(105—107 111) 18(106) 19(107 111) 20(105—107 111) 22 23
Dannenberg, J.J.      17 19 20(117 123) 23
Dantanarayana, A.P.      388 391(96f) 470
Danzo, BJ.      845(180 182 183) 865
Das, G.      527(81) 545
Das, G.P.      15(80 85) 22
Das, K.G.      401(130) 472
Das, P.K.      336(31—37) 337(33 35) 354 355
Dauben, W.G.      274(24) 276(27a 27b) 320 377 378(69a 69b) 407(156a) 469 473 565(67) 582(107a) 601(172) 613 614 616
Dauber, P.      153 159 161(22) 170
Daucher, B.      949 959(61) 975
Davidson, E.R.      11(52) 13(52 66) 14(72) 21 22
Davidson, J.M.      660 662(28) 680
Davies, M.      657(13a) 679
Davis, B.H.      503(51) 505
Davis, J.T.      419(165e) 474
Dawe, E.A.      237 238 245(287) 261
Dawson, J.I.      160(68) 171
Dawson, M.I.      808(84) 863
Day, A.C.      289 293(58) 322
Day, C.A.      289(59b) 322
De Carvlho, M.-E.      899(53) 923
De Clerq, P.      507(1) 544
de Dios, A.      440 442(244d) 477
de Groot, A.      374(50 51) 469
de Julien de Zelicourt, Y.      102(97) 110
De Keukeleire, D.      264(1c) 319
De Kok, A.J.      119(16a 16b) 146
De Koning, L.J.      236(274) 260
de Korswagen, C.      180 181(65) 255
de la Pradilla, R.F.      440 442(244d) 477
De Lera, A.R.      268(15a) 320
de Maijere, A.      903 904(78) 924
De Maio, G.R.      35 36(46d) 62
de Mayo, P.      268(14e) 311(106a 106b) 313(14e) 320 323
De Medeiros, E.F.      459(300a 300d) 461(300a) 462(300d) 479
De Meijeie, A.      52(141) 65 180 181(72) 256
de Meijere, A.      27 28(9) 42(9 92) 61 63 180(54 62 66) 181(54 86) 183(62 86 124) 184(140) 225(211) 255—257 259 433(208b 213) 434(209b) 436(224a 224b) 476 477 562(58) 605(184) 609(196) 613 616 617
de Ochoa Echaguen, C.      18(133) 23
de Ortiz Montellano, P.      913(145) 925
Deana, A.A.      827(144) 864
Debromination, as synthetic procedure for conjugated dienes/polyenes      366 367
Decadienes      see “Dispirodecadiene”
Decarboxylatiou, double      666
Decarboxylative elimination, as synthetic procedure for conjugated dienes/polyenes      372—374
Declerq, J.-P.      949(58) 975
Decorzaht, R.      511(24b 27) 544
Decorzani, R.      375(56b) 469
Decorzant, R.      457(293) 479
Decosta, D.L.      280(39) 321
Defauw, J.      533(101 103) 535(107) 546
DeFrees, D.J.      32(25) 62 738(22) 750
DeFuria, F.      910(119) 924
Degenhardt, C.A.      181(84) 256
Degenhardt, C.R.      225(213) 259
DeGeorge, J.J.      824(125) 864
Dehennin, L.      500(44) 505
Dehn, J.S.      498(39) 505
Dehydration, as synthetic procedure for conjugated dienes/polyenes      366—368
Dehydrobromination, as synthetic procedure for conjugated dienes      364—366
Dehydromesylation, as synthetic procedure for conjugated dienes      368 369
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