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Авторизация |
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Поиск по указателям |
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Rappoport Z. (ed.) — The Chemistry of Dines and Polyenes (vol. 1) |
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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
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