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Авторизация |
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Rappoport Z. (ed.) — The Chemistry of Dines and Polyenes (vol. 1) |
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Предметный указатель |
Busier, W.R. 343(89) 356
Buss, A.D. 415(168a-c 169a 169b) 474
Buss, V. 141(50e) 147
Butadiene monoepoxide, deuterium-labelled, synthesis of 777 778
Butadienes (see also “1 “t-Butyl-1 “2 “Methyl-1 “Phenyl-1 “Polybutadienes”)
Butadienes, cyclization of 508
Butadieuyl radical cations 338
Butatrienyl cations 883—885
Butatrienyl halides, solvolysis of 883—885
Butenandt, A. 454 455(278b) 479 896(36) 923
Butenes, acidity of 736
Butenko, O.Y. 180(52) 255
Buxton, G. 353(152) 357
Buxton, G.V. 328(12) 354
Buzelaar, P.H.M. 51(137c) 64
BystrBm, S.E. 662 663(33a) 666(38 40) 680
Bystrom, S. 366 367(28d) 468
Bywater, S. 745(71) 751
Cabiddu, S. 627 635(36b) 650
Cabral, J. 747(56) 751
Cacchi, S. 433(215a) 434(209a) 476
CadioH, B. 26(3) 61
Cahiez, G. 457(290) 479
Caine, D. 282(47a 47b) 321 415 421 460(171b) 474
Cais, M. 361 364(1) 467
Calabrese, J. 949(63) 975
Calabrese, J.C. 942(33) 975
Calciferols 119
Caldwell, DJ. 112 117(lc) 119(18) 120 133(1c) 146
Caldwell, RA. 739(32) 750
Came, I. 381(81b) 470
Cameron, J.F. 808(84) 863
Caminati, W. 5(38d) 21 33(30) 62
Cammers-Goodwin, A. 511(18) 544
Camp, M.R.de 562(60) 613
Campbell, J.B.Jr. 415 421(171c) 432(207b 207c) 446(256) 474 476 478
Campbell, S. 388 390(96c) 470
Cannizzaro, S. 281(40c) 321
Cannizzo, L.F. 426(184b) 475
Cantrell, T.S. 308(101g) 313(109a) 323 324
Caple, G. 510(12) 544
Caporusso, A.M. 117 118 135(13) 146
Capsantin, analysis of 503
Carbene insertion reactions, in synthesis of conjugated dienes 465
Carbochlorination 673
Carbocyclization 672
Carbon dioxide, extrusion of, in synthesis of conjugated dienes 401
Carbon monoxide, extrusion of, in synthesis of conjugated dienes 401
Carboxylate anions, decarboxylation of 736
Carcinoma, mechanism of treatment of 776
Carder, R.W. 289(59b) 322
Cardfflo, M.J. 44(100) 63
Carless, H.A.J. 297(73b) 298(73b 77c) 322
Carmody, M.A. 298(78) 322
Caronna, T. 648(94) 652
Carotenoids, analysis of 493 494 501—504
Carotenoids, chirality of 137—141
Carotenoids, radiolysis of 337 338
Carotenoids, Raman spectra of 166 168
Carpenter, B.K. 337 338(50) 355
Carpenter, J.E. 17 18(99) 22 32(24) 62
Carpita, A. 452(269c) 478
Carr, R.V.C. 915(159) 925
Carrasco, M.C.S. 430(192 193b) 475
Carreira, L.A. 53(153) 65 161 162(69) 171
Carretero, J.C. 393(104) 471
Carrupt, P.-A. 134(43) 147 184(158) 258
Carry, J.-C. 406(149) 472
Carsky, P. 242(291 292) 261
Casas, R. 17 20(122) 23
Casey, C.P. 432(205 206b) 476
CASPT2 method 11—14
Castano, A. 672 673(55) 680
Castedo, L. 415 421(171d) 438 439(234b) 474 477
Castiglioni, C 150 166(6) 169
Cativiela, C 17 19 20(129) 23
Catt, J.D. 827(142) 864
Cattel, L. 823(121 122) 864
Cavazza, M. 287(52c) 322
Cave, R.J. 11(52) 13(52 66) 14(72) 21 22 248(305) 261
Cecere, M. 624 625 631(17) 648(17 94) 650 652
Cederbaum, L.S. 211(189) 258
Ceita, L. 381(82) 470
Cerati, A. 647(90) 652
Cerfontain, H. 297(74) 322
Cerorubenoll 315 316
Ceruti, M. 823(121 122) 864
Cervelrati, R. 53 54(159) 65
Cervini, L.A. 536(108) 546
Cha, DA. 895 896(30) 923
Cha, J.K. 897(43) 923
Chabardes, P. 394(105e) 471
Chabert, P. 412(161c) 473
Chachaty, C 339(66) 355
Chadwick, R.R. 11 13(47 48) 21 153(27) 159 160(27 66) 170 171
Chaffee, K. 315(112b) 324
Chakraborty, T.K. 420(166c) 423(172c) 440(249) 474 478
Chakraborty, V. 434(2091) 476
Challacombe, M. 32(25) 62
Chamberlain, N.F. 39(79) 63
Chamberlin, A.R. 416(164a) 473 536(108) 546
Chambers, L. 394 396(106a) 471
Chamey, E. 112(la) 114 115(9) 117(la 9) 119(20—24) 120(la 22 23) 122(23) 126(36) 133(la) 134(36) 144(22) 146 147
Champagne, B. 15(84 87) 16(87) 22
Chan, C. 450(261a 262) 478
Chan, L.M. 818(104) 863
Chan, T.-H. 424(178b 179a) 425(179a) 475
Chan, T.-T. 378(72b) 469
Chan, T.-Y. 378(72a) 469
Chan, T.H. 424(178g) 475
Chan, W.K. 141(50a) 147
Chance, R.R. 157(43) 166—168(97) 170 171
Chandrasekaran, S. 894(24) 911(134) 923 925
Chandrasekharam, M. 463(302 304) 480
Chang, C.-T. 628(44) 651
Chang, E.S. 812(91) 863
Chang, H.M. 242(292) 261
Chang, S. 602(178a) 616 900(63) 923
Chang, S.Y. 398(120b) 471
Channamallu, K. 86(52) 108
Channing, MA. 824(123) 825(126) 826(123) 864
Chanon, M. 232(224) 259
Chapiro, A. 345(98 99) 346(102) 356
Chapman, O.L. 81(35a) 107 268(12b 14a 14f) 313(14a 14f) 320
Chappuis, J.L. 119 124 125(26) 147
Chapuis, C. 592(142) 615
Charbonneau, G.P. 53(154) 65
Charge-transfer interactions, parameterization of 712
Charles, N.R. 315(112a) 324
Charlesby, A. 347(113 115 116) 350(113) 356
Charlton, J.L. 399(124h 124i) 401(124i) 472
Charton, B.I. 689(23) 704(37) 710 711(49) 712(49 51 53) 714(51 53) 731 732
Charton, M. 688(17 18) 689(22—24) 690 691(22 25) 692(22 27) 698(27) 699(25 28) 701(24 25 27) 704(37—39) 705(42) 706(43—45) 707(45 46) 708(45 47) 709(47) 710(24 25 27 47 49 75) 711(49 50 52) 712(49 51—53) 714(24 25 27 51 53) 727(50) (26) 731 732
Charumilind, P. 182(103) 256
Chase, C.E. 268(13) 311(105 107) 313(13) 320 323
Chastel, R. 99(88) 110
Chau, A.S.Y. 892(2) 922
Cheeseman, J.R. 32(25) 62
Chemiak, EA. 498(40) 505
Chemical derivatization 496—499
Chemical ionization, in structure determination of dienes/polyenes 494 495
Chemin, D. 438(232) 455(283b) 477 479
Chen, C.-H. 424 425(179c 179d) 475
Chen, C.E. 31(21) 62
Chen, C.S.H. 627 636(31) 650
Chen, H.-C. 399(127) 472
Chen, J. 308(102) 323
Chen, M.-Y. 627 631(32) 650
Chen, P. 213(192) 259
Chen, P.M. 791(42) 862
| Chen, R.L. 418(165b) 474
Chen, S. 394(108a) 471
Chen, W. 32(25) 62
Cheng, K.-F. 378(72a 72b) 469
Cheong, K.K. 119(18) 146
Cherest, M. 17 19 20(115) 23
Cheson, R.M. 548 564(3) 611
Cheung, H.-C. 394 396(106b) 471
Chiang, C.C. 40(86) 63
Chiang, J.F. 38 42(59) 52—54(146) 63 65
Chiba, Y. 449(268a) 478
Chickos, I.S. 70(4—6) 104
Chida, N. 433(212a) 476
Chidambaram, N. 911(134) 925
ChiMna, Z.N. 351(138) 357
Chiou, D.-M. 874(25) 886
Chiral carotenoids 137—141
Chiral dienes, intrinsically chiral 117—132
Chiral dienes, origin of optical activity and 114—117
Chiral dienes, owing their chirality to a dynamic twist 132 133
Chiral dienes, owing their chirality to dissymmetric perturbation 133—137
Chiral oligoenes 141
Chiral polyalkynes 141
Chirico, R.D. 81(42a 42b) 107
Chirstmann, K.-F. 407(152a 152b) 473
Chittattu, G. 528(82) 545
Chiusoli, G.P. 466(313e) 480
Chloramines, addition to dienes 648
Chloroacyloxylation 663—665
Chloropalladation 672
Chloroprene, polymerization of, radiation-induced 344
Chlorotriary lallenes, photolysis of 870 871
Chlorotriary lallenes, solvolysis of 871—873
Choe, J.-I. 41 42(91) 63
Choi, S. 4—6(35) 21
Choi, Y.S. 14(74) 22
Chong, C.N. 500(46) 505
Chou, S.S.P. 395(112c) 471
Chou, T.-C. 368 369(31e) 468
Chou, T.-S. 395(112b 112c) 397(115) 398(120a 120b) 399(127) 471 472
Choudary, B.M. 453(276c) 479
Choudhry, S.C. 783 805 809 834(27) 862
Chow, A. 747(57) 751
Chow, T. 182(110) 257
Choy, W. 419(165e) 474 910(121) 924
Christensen, D.H. 162—165(86) 171
Christensen, R.L. 14(74) 22
Christl, M. 180 181(67 68) 256
Christoph, G.G. 49(127) 64 225(211) 259
Chromate-based oxidants 898
Chrysanthemates, synthesis of 278 279
Chrysanthemic acid, synthesis of 278 280
Chuang, C.-P. 522(61) 545
Chum, P.W. 538(112) 546
Chumey, K.L. 69(3) 104
Chung, A.L.H. 102(99b) 110
Chung, J.Y.L. 450(262) 478
Chung, S.K. 657(14) 680
Chung, T.-C. 158(44) 170
Chupka, WA. 179(24) 255
Chwang, W.K. 717(57) 732
Ciardelli, F. 141(48) 147
Ciattini, P.G. 433(215a) 476
Cibura, G. 877 879(35) 886
Ciganek, E. 511(21) 544 566(80) 570(80 81) 613
Cimiraglia, R. 287(52c) 322
Ciolowski, J. 32(25) 62
Ciprostene, tritium-labelled, synthesis of 818
Circular dichroism (CD) spectroscooy 112 116 118
Circular dichroism (CD) spectroscooy of carotenoids 138—141
Circular dichroism (CD) spectroscooy of distorted dienes 129
Circular dichroism (CD) spectroscooy of planar dienes 134—137
Circular dichroism (CD) spectroscooy of polyalkynes 141
Circular dichroism, contributions to 123—126
cis-Allo-ocimene, thermochemistry of 88 89
Cisoid conformation, of conjugated dienes 112 113 120—122 126
Citterio, A. 621 622(7 8) 631(57) 646(7) 647(89 90) 649(8) 650—652
Ciula, J.C. 734(4) 750
Claesson, A. 368(37) 468
Claisen rearrangement, as synthetic procedure for conjugated dienes 406
Claisen rearrangement, effect of pressure on 596 598
Claisen rearrangement, mechanism of, isotope effect studies of 776 854—858
Clanton, JA. 845(180 183) 865
Clar, J.E. 381(81b) 470
Clardy, J. 182(103) 183 184(128) 256 257
Clardy, J.C. 184(141 142) 257
Clark, K.B. 179(36) 255
Clark, P.A. 183(125) 257
Clark, R.J.H. 151(16) 170
Clark, T. 747(61) 751
Clarke, R. 498(36) 505 907(104) 924
Claspy, P.C. 236(244) 260
Clathrates, tunnel 343
Claus, K. (216) 866
Claus, K.H. 38(73) 63
Clayden, J. 415(168d) 474
Clayton, J.D. 895(32) 923
Cleavage reactions, oxidative 655 658 660 891
Clementi, E. 4(12) 15(79) 21 22 31(15 16) 61 166(109) 172
Clennan, E.L. 289(59a) 322 915(153) 925
Clericuzio, M. 133 134 137(41c) 147
Clive, D.L.J. 408(154c) 473 528(82) 545
Closed-shell molecules, singlet ground configuration for 197 198
Clough, J.M. 415 421(171a) 474
Clough, R.L. 347(121 122 124) 356
Clozepine, tritium-labelled, synthesis of 821 822
CNDO/2 calculations, for 1,3-butadiene 120
CNDO/S calculations, for 1,3-butadiene 120
CNDO/S calculations, for steroidal models 122 123
Coates, R.M. 859(236) 867
Cobum, J.F.Jr. 84(45) 107
Cockerill, A.F. 364(20a) 468
Cocrystallization 34
Coggiola, I.M. 791(39) 862
Cohen, M.P. 559(51) 613
Cohen, N. 530(90) 545
Cohen, T. 432(204) 476
Colapret, K.A. 772(24) 774
Colchicine, photocyclization of 268 269
Colchinols see “N-Acetylcolchinols”
Cole, A.R.H. 5(40) 21 158 159(51) 170
Cole, R.H. 6(41) 21
Cole-Hamilton, D.J. 498(36) 505 907(104) 924
Collins, C.J. 849(198) 866
Collman, J.P. 899(56) 923
Colpa, J.P. 639(73) 651
Colson, St.D. 179(24) 255
Colvin, E.W. 424(178k) 475
Come, J.H. 313(110a 110b) 324
Comelise, J. 870(6) 886
Comelisse, J. 141(49) 147
Comita, P.B. 405(145) 472
Complete Active Space SCF (CASSCF) scheme 3 8 11 13 15 17
Composite parameters 689
Compton, D.A.C. 161(77) 171
Condon, S. 378(73) 469 898(50) 923
Condon, S.M. 440 443(245a) 477
Condroski, K.R. 631(61) 651
Configuration interaction (CI) method 3
Configuration interactions 214
Conjugated dienes 68
Conjugated dienes, addition reactions of 609 610
Conjugated dienes, anodic oxidation of 753—759
Conjugated dienes, cathodic reduction of 768 769
Conjugated dienes, chirality of 114—137
Conjugated dienes, conformation of 112—114 117 120—122 126 128—131 133—137 141
Conjugated dienes, cyclization of 508
Conjugated dienes, cyclization of photochemical 268 269
Conjugated dienes, oxidation of, palladium-catalysed 661—677
Conjugated dienes, oxidation of, with metal salen complexes 900 901
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