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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
Zhuravleva, E.B.      609(192a 192b) 617
Zhuravskaya, E.V.      346 347(105) 356
Ziegler, F.      434(209f) 476
Ziegler, F.E.      854(211) 866
Ziegler, K.      510(15a) 544
Ziegler, L.D.      153(23) 170
Zielinska, A.      (215) 866
Zielinski, J.      843 844(178) 865
Zielinski, M.      802(70) 826(135—139) 863 864 853(209) (215) 866
Ziindorf, W.      931 940 941(9) 974
Ziller, C.H.      465(310c) 480
Ziller, H.      114 115(9) 117(9 15) 119(20 21) 126 134(36) 146 147
Ziller, J.      539(115) 546
Zimmer, H.      718(60) 732
Zimmer, O.      958(79) 976
Zimmerman, A.H.      739(34 35) 750
Zimmerman, H.E.      277(32a 32b) 281(41a 43) 320 321
Zimmerman, W.T.      377 378(69b) 469
Zimmermann, H.      185(160) 258
Zimmermann, H.E.      48(120) 64
Zimny, B.      548(14) 568(73) 584 585(112) 599(163) 602(180) 608(188) 611 613 614 616 617
Zin, P.      417(164c) 473
Zinger, B.      758(9) 774
Zipkin, R.      415 421 460(171b) 474
Zipkin, R.E.      454(279a-c) 479
Zipse, H.      621 631(10) 650
Zirconocene, in cyclizations      539 540
Zoch, H.G.      949(58) 975
Zoebisch, E.G.      630(48) 651 599(163) 602(180) 608(188) 611 613 614
Zott, H.      349(129) 357 616 617
Zsigmond, A.      668(48a 48b) 680
Zuccarello, G.      375(58) 469
Zuendoif, W.      931 940 941(9) 974
Zueva, A.F.      352(142) 357
Zverev, V.V.      179 180(40) 255
Zwanenbuig, B.      627 635(36c) 650
Zwick, G.      920(194) 926
Zwitterionic intermediates, in photo-rearrangements      281—290 293 294
[3]Radialenes      928
[3]Radialenes in donor-acceptor complexes      945
[3]Radialenes, catalytic hydrogenation of      940
[3]Radialenes, colour of      937 940 943
[3]Radialenes, cycloadditions of      941
[3]Radialenes, functionalized      936—939
[3]Radialenes, oxidation of      941 942
[3]Radialenes, photoionization of      941
[3]Radialenes, protonation of      940 941
[3]Radialenes, reduction of      937 941—943 945
[3]Radialenes, structure of      55—57 60 61
[3]Radialenes, synthesis of      931—940
[3]Radialenes, synthesis of by eyclotrimerization      936
[3]Radialenes, synthesis of from 1,1-dihaloalkenes      935
[3]Radialenes, synthesis of from bis(4-hydroxyphenyl)cyclopropenones      938
[3]Radialenes, synthesis of from hexachlorocyclopropane      940
[3]Radialenes, synthesis of from tetrachlorocyclopropene      939
[3]Radialenes, thermal stability of      931 937
[3]Radialenes, with quinoid substituents      935—937
[4,4,4]Propellahexaene, structure of      45 46
[4]Radialenes      928
[4]Radialenes, colour of      946
[4]Radialenes, cycloadditions of      955 956
[4]Radialenes, cyclopropanation of      956 957
[4]Radialenes, electrophilic addition to      957 958
[4]Radialenes, isomerization of      958
[4]Radialenes, phenyl-substituted      945
[4]Radialenes, redox reactions of      959 961
[4]Radialenes, ring opening of      958
[4]Radialenes, structure of      55 57 58 60 61
[4]Radialenes, synthesis of      945—954 963
[4]Radialenes, synthesis of by cyclodimerization of cumulenes/trienes      947—951
[4]Radialenes, synthesis of from bis(l-diazo-2-oxoalkyl)silanes      949
[4]Radialenes, synthesis of from cyclobutanes      944—946
[4]Radialenes, synthesis of from dihalides      952 953
[4]Radialenes, thermal stability of      954 955
[5]Radialenes      928
[5]Radialenes, electrochemistry of      963
[5]Radialenes, structure of      55 56 58 60 61
[5]Radialenes, synthesis of      961—964
[6]Radialenes      928
[6]Radialenes as ligands      968
[6]Radialenes, cycloadditions of      967 969
[6]Radialenes, cyclopropanation of      967 968
[6]Radialenes, electrophilic addition to      966
[6]Radialenes, epoxidation of      968
[6]Radialenes, photoisomerization of      968
[6]Radialenes, stability of      965
[6]Radialenes, structure of      55 56 58 60 61
[6]Radialenes, synthesis of      951 964 965
[6]Radialenes, thermal rearrangement of      966
[7]Radialenes      970 971
[8]Radialenes      970 971
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
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