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

Àâòîð: Rappoport Z. (ed.)

Àííîòàöèÿ:

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.


ßçûê: en

Ðóáðèêà: Õèìèÿ/

Ñòàòóñ ïðåäìåòíîãî óêàçàòåëÿ: Ãîòîâ óêàçàòåëü ñ íîìåðàìè ñòðàíèö

ed2k: ed2k stats

Ãîä èçäàíèÿ: 1997

Êîëè÷åñòâî ñòðàíèö: 1054

Äîáàâëåíà â êàòàëîã: 20.04.2006

Îïåðàöèè: Ïîëîæèòü íà ïîëêó | Ñêîïèðîâàòü ññûëêó äëÿ ôîðóìà | Ñêîïèðîâàòü ID
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Ïðåäìåòíûé óêàçàòåëü
Pilet, O.      185(163) 258
Pillai, K.M.R.      844 845(177) 865
Pimentel, G.C.      233(231) 260
Pindur, U.      591(135) 615
Pinke, P.A.      466(313a) 480
Pinkos, R.      575(92b) 614
Pinos, R.      252(309) 261
Pinto, I.      629(45) 651
Pinto, I.L.      458(294) 479
Piocos, EA.      337(46) 355
Piotti, M.E.      456(287) 479
Piper, S.E.      399(126) 472
Pirkle, W.H.      268 313(14d) 320
Pirrung, M.C.      282(44a) 321
Piscopio, A.D.      440(249) 478
Piseri, L.      166(115) 172
Piskala, A.      407(152b) 473
Pistorius, R.      643(81c) 651
Pitt, G.A.J.      783(30) 862
Pitteloud, R.      520(55 57) 545
Plalt, K.L.      364 365(23b) 468
Planar diene rule      136
Planar dienes      114 117
Planar dienes s-cis      132—134 141 142
Planar dienes s-trans      135—137 141 142
Planter, R.D.      918(175) 926
Plastic phases      46
Platsch, H.      185(164) 258
Plemenkov, V.V.      179(40) 180(40 52) 255
Plieninger, H.      570(83) 602(176 177 179) 614 616
Pliss, E.M.      180(73) 256
Ploteau, C.      675(59) 681
Poddington, J.      213(193) 259
Pododensin, A.      90(64) 108
Poeth, T.      432(204) 476
Poggi, G.      119(25) 147
Poklukar, N.      920(199) 926
Pokrovskaya, I.E.      497(33) 505 920(192) 921
Polarizability      15
Polarizability bond-bond      213
Polbom, K.      57(169) 65 949(59) 975
Pollack, R.M.      97(79) 109
Pollack, S.K.      99(90) 110 738(22) 750
Pollard, R.      279(38c) 321
Pollmann, M.      578(97) 614
Polyacetylene, absorption spectrnm of      158
Polyacetylene, quantum-chemical calculations for      9 10
Polyacetylene, radiation chemistry of      352 353
Polyacetylene, Raman spectra of      166 169
Polyacetylene, structures of      168
Polyacetylene, thermochemistry of      87
Polyalkynes      (see also “Polyacetylene”)
Polyalkynes chirality of      141
Polyalkynes, radiation chemistry of      352—354
Polybutadienes, formation of      343
Polybutadienes, radiation chemistry of      346—351
Polycyclic dienes, oxidation of, with osmium tetraoxide      895—897
Polycyclic dienes, oxidation of, with ozone      921
Polycyclic dienes, oxidation of, with peroxo compounds      906
Polycyclic dienes, oxidation of, with ruthenium tetraoxide      898
Polycyclic dienes, oxidation of, with triplet oxygen      918 919
Polycyclic dienes, structure of      41—50
Polycyclic polyenes, structure of      41—50
Polyene macrolides, analysis of      500 501
Polyenes      (see also “$\alpha</a></span> <span class=subjpages><a href= “Heptaenes” “Hexaenes” “Nonaenes” “Pentaenes” “Spiropolyenes” “Tetraenes” “Trienes”
Polyenes, absorption spectra of      155—158
Polyenes, acidity of      748 749
Polyenes, buried      68
Polyenes, cathodic reduction of      770—773
Polyenes, conformation of      166—169
Polyenes, electronic spectra of      236—238
Polyenes, electronic structure of      154
Polyenes, fluorescence spectra of      156 157
Polyenes, long, excited states of      14 15
Polyenes, long, geometry/force fields for      9 10
Polyenes, PE spectra of      178 183—185
Polyenes, radical additions to      620—627
Polyenes, Raman spectra of      166—169
Polyenes, regioselectivity in      630—634
Polyenes, synthesis of, $\sidset{^{119m}}{}Sn$-labelled      847 848
Polyenes, synthesis of, $\sidset{^{11}}{}C$-labelled      824—826
Polyenes, synthesis of, $\sidset{^{125}}{}I$-labelled      845 847
Polyenes, synthesis of, $\sidset{^{13}}{}C$-labelled      802—806
Polyenes, synthesis of, $\sidset{^{14}}{}C$-labelled      827 829—841
Polyenes, synthesis of, $\sidset{^{15}}{}N$-labelled      807
Polyenes, synthesis of, deuterium-labelled      776—802
Polyenes, synthesis of, tritium-labelled      808—818 821—824
Polyenoates      see “Hexaenoates” “Trienoates”
Polyenoic acids      see “Hexaenoic acids” “Tetraenoic
Polyenyl radicals      619 625
Polyenyl radicals, reactions of      627—630
Polyenyl radicals, reactions of regioselectivity in      634—643
Polyhomoalrylie fatty acids, $\sidset{^{11}}{}C$-labelled, synthesis of      824 825
Polyisoprene, formation of      344—346
Polyisoprene, radiation chemistry of      346—351
Polymerization      (see also “Copolymerization”)
Polymerization radiation-induced      343—346
Polymers, radiolysis of      346—351
Polymers, radiolysis of, effect of oxygen on      347
Polymorphism      29 46
Pomerantz, M.      84(45) 107
Pommer, H.      407(150f 153) 473
Pong, R.G.S.      313(108a 108b) 324
Pontikis, R.      782(23) 861
Pople, J.A.      3(6) 20 32(25) 51(136a) 62 64 78(27) 106 183(114) 197(169) 211(114) 257 258 747(61) 751
Popov, E.M.      158(58) 171
Porco, J.A.Jr.      297—299(73c) 301(85a 85b 86) 304(73c) 322 323
Porphyrins      (see also “Metalloporphyrins” “Octamethylporphyrin”)
Porphyrins in aerobic oxidation      667
Porter, B.      457(292) 479
Porter, N.A.      633 640(62) 651 917(170 171 174) 925
Posner, G.H.      366(29b) 406(149) 468 472 592(138) 615
Posner, T.      631(59) 651
Poss, A.J.      417(164c) 473
Post, B.      52 53(148) 65
Postemak, T.      892(11) 922
Potential energy functions      6
Potential surfaces      6 7
Potier, P.      368 369(31b) 380(79 80) 468 470
Potts, W.J.      169(123) 172
Poutsma, M.L.      636(65) 651
Powell, J.      677(61a) 681
Powell, K.A.      892(9 10) 922
Powell, W.S.      411(155e) 473
Powner, T.W.      511(26) 544
Prakash, S.R.      843(176) 865
Prandi, J.      912(139) 925
Prasad, L.      338(59 60) 355
Prasad, P.N.      15 16(81) 22
Precalciferol, ring closure of, photochemical      268 271
Prednisolone suleptanates, $\sidset{^{14}}{}C$-labelled, synthesis of      842 843
Prednisolone, deuterium-labelled, synthesis of      799 800
Prednisone, deuterium-labelled, synthesis of      799 800
Prestwich, G.D.      809 810(87a 87b) 812(90) 838(163) 863 865
Preuss, H.      252(308) 261
Preuss, T.      181 183(86) 256 903 904(78) 924
Price, R.      807(79) 863
Prileschajew, N.      901(67) 923
Prins, W.L.      395(114b) 471
Prinzbach, H.      182(102 108 112 113) 184(108) 185(112 160) 236(266) 252(266 309 310) 256—258 260 261 466(312a 312b) 480 575(92a 92b) 614
Prokopeko, V.A.      397(116c) 471
Propargyl cations      873
Propargyl halides, solvolysis of      874
Propelladienes      90
Propellanes      90
Propenes      (see also “Cyclopropenes”)
Propenes, cidity of      736 739
Pross, A.      620(4) 650 738(22) 750
Prostaglandins, synthesis of, biomimetic      639 640
Prostaglandins, synthesis of, isotopically labelled      776 784 786—788 793—799 812—818 827
Protoanemonin in Diels — Alder reaction      18
Proton affinity, measurement of      99
Proton transfer, rates of, isotope studies of      734
Prudent, N.      17 19 20(115) 23
Pruesse, T.      860(241) 867
Prugh, J.D.      827(144) 864
Pryzbyla, C.A.      894(23) 922
Psaume, B.      376(62) 469
Pseudomonas putida in synthesis of conjugated dienes      465
Pseudoscopine, synthesis of      665
Pucci, S.      158(55) 171
Pugh, D.      15(89) 22
Pujol, D.      639(78) 651
Pulay, P.      4(14 31) 5 8—10(31) 21 152(19) 162(92) 170 171
Pumilotoxin, synthesis of      678 679
Pupyshev, V.I.      4 5 7(19) 21 162 164(91) 171
Purmort, J.I.      747(62) 751
Puzicha, G.      805(76) 863
Pyne, S.G.      394(108a) 471
Pyridinium sulphonate, ring opening of      460
Pyridones, Diels — Alder reaction of      580 589
Pyridones, [4+4]photocycloaddition of      308 309
Pyrones      (see also “Dewar pyrones” “2-Hydroxyalkyl-4-pyrones” “3-Hydroxy-4-pyrones”)
Pyrones, Diels — Alder reaction of      580 588
Pyrones, photorearrangement of      287—289
Pyrones, [4+4]photocycloaddition of      310—313
Pyrrolcarboxylates, $\sidset{^{15}}{}N$-labelled, synthesis of      807
Pyrroles      (see also “3-Hydroxyalkylpyrroles”)
Pyrroles, Diels — Alder reaction of      575 580 586
Pyrrolizidine alkaloids, synthesis of      677
Pyrylium ions      (see also “4-Hydroxypyrylium ions”)
Pyrylium ions, ring opening of      459 461 462
Pyun, H.J.      859(236) 867
QCISD(T) level      17
Qi, Y.      86(50) 108
Qin, X.Z.      248(304) 261 337(44 49) 338(49) 355
Qninone monoketals, photorearrangement of      282
QSCR      720 721 723
QSPR      721—727
QSRR      716—720 723—725
Quinkert, G.      265(7 9) 266(10a 10b) 319 399(124f) 472
Quinodime thanes      see “o-Quinodime thanes” “Xylylenes”
Quintanilha, A.      917(168) 925
Quintard, J.P.      446(252) 478 675(59) 681
Quintata, C.A.      347(122) 356
Raaen, V.F.      848 849(195) 866
Rabideau, P.W.      81 88(37) 107
Rabinovich, D.      40(88) 63
Rabjouh, N.      901(65) 923
Rablen, P.R.      4 6(22) 21
Raby, P.      338(64) 355
Rachdi, F.      911(133) 925
Rademacher, P.      58(185) 65 184(137) 257
Radialene ketones      951 963
Radialenes      (see also “Heteroradialenes” “Naphtharadialene” “Permethylradialenes” “Trimethylsilylethynylradialenes”)
Radialenes expanded      929
Radialenes expanded, synthesis of      970—973
Radialenes, nomenclature of      927—930
Radialenes, significance of      930
Radical addition      619—649
Radical addition intramolecular      627
Radical addition, regioselectivity of      630—634
Radical cations, electronic doublet states of      175
Radical cations, electronic structure of, by electronic spectra      229—239
Radical cations, electronic structure of, by PE spectra      175—228
Radical cations, electronic structure of, by theoretical methods      240—243
Radical cyclization      627—630 633 634 646
Radical halogenation      636
Radical pair mechanism      639
Radical reactions      (see also “Radical addition” “Radical “Radical
Radical reactions chain      619 620 626 642
Radical reactions nonchain      644—649
Radical recombination      620 639 641 643
Radical scavengers      327 328
Radicals, initiator-derived, addition to dienes      624
Radiolysis of dienes in aqueous solution      327—334
Radiolysis of dienes in non-aqueous solvents      334—339
Radiolysis of water      327
Radom, L.      3(6) 20 78(27) 106 183 211(114) 257 620(4) 650 738(20 22) 750
Radonovich, L.J.      36(52) 62
Radwan-Pytlewski, T.      394(105c) 471
Rafel, J.      17 19 20(114) 23
Rafel, S.      17 19 20(113) 23
Raghavachari, K.      32(25) 62
Raghavan, N.V.      336(31) 354
Rahm, A.      590(127) 615
Raimondi, L.      17 18 20(104) 22 852 853(207) 854(207 210) 866
Rainbow, L.J.      459(296) 479
Raine, B.C.      99(90) 110
Raitery, M.I.      804(74) 863
Rajadurai, S.      336(37) 355
Rajaram, J.      453(276b) 479
Ramachandran, K.      457(292) 479
Raman spectroscopy      151—153
Raman spectroscopy of 1,3-butadiene      158—161
Raman spectroscopy of polyenes      162—169
Ramanathan, H.      280(39) 321
Ramasubbu, A.      540(118a-c) 546
Ramberg, L.      374(52a) 469
Ramberg-Backlund reaction, as synthetic procedure for conjugated dienes/polyenes      374 375
Ramesh, S.      417(164c) 473
Ramirez-Munoz, M.      375(56a) 469
Ramm, P.J.      838(164) 865
Ramondenc, Y.      382(83f 84) 384 419(83f) 470
Raney, K.D.      905(94) 924
Rankin, D.W.H.      179(43) 255
Rannela, E.      594(147) 615
Rao, Ch.S.      463(302 303b) 480
Rao, S.A.      431 432(201) 476
Raphael, R.A.      405(139) 472
Rapoport, S.I.      824(125) 864
Rapp, G.A.      717(58) 732
Rappoldt, M.P.      268(16a) 320
Rappoport, Z.      278(34c) 321 673(57b) 681 869(1 2) 872(22) 886
Rasmussen, R.S.      158(48) 170
Rathunde, R.A.      155(33) 170
Ratovelomanana, V.      438 439(234a) 452(269a) 454(280) 477—479
Rauch, M.U.      902(73) 924
Rauchschwalbe, G.      746(59) 750(75) 751
Rauk, A.      114 119(7) 120(28) 146 147
Raulins, N.R.      276(29a) 320
Ravindran, K.      310(104) 323
Rawley, A.G.      407(150e) 473
Rawlinson, D.J.      648(93) 652
Raybock, S.A.      899(56) 923
Raymo, F.M.      576(94e) 614
Rayner, CM.      910(118) 924
Reaction volume      548—552
Reaction volume relationship with ring size      603 608 609
Reay, P.P.      791(43) 862
Receptor interactions, determination of mechanism of      776
Reddy, G.S.      426(184a) 475
Reddy, M.P.      464(306) 480
Reddy, S.M.      136 137(45a 45b) 147
Reddy, V.P.      602(175) 616
Redel, J.      435(220) 476
Ree, K.H.      56(165b) 65
Reed, A.E.      32(24) 62 742(41) 750
Reed, J.W.      278(34a) 321
Reed, K.L.      906(100) 924
Reed, R.I.      486(13) 504
Rees, C.W.      457(291) 479
Reetz, M.T.      17 19 20(118) 23 184(156) 258
Reeves, R.L.      378(70c) 469
Reffly, J.      285(49d 50) 321 895(34) 923
Regioselectivity in Diels — Alder reaction      19
Regioselectivity in radical additions      630—634
Regioselectivity in reactions of polyenyl radicals      634—643
Reglier, M.      541(119) 546 653(4 5) 657(16—19) 658(4 16) 679 680 919(187) 926
Rehner, J.      347(114) 356
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