-
1
-
-
0002658779
-
-
Part I: T. Ueno, H. Toda, M. Yasunami, and M. Yoshifuji, Chem. Lett., 1995, 169.
-
(1995)
Chem. Lett.
, pp. 169
-
-
Ueno, T.1
Toda, H.2
Yasunami, M.3
Yoshifuji, M.4
-
5
-
-
0003610755
-
-
VCH, Weinheim
-
J. F. Liebman, A. Greenberg, and W. R. Dolbier, Jr., "Fluorine-Containing Molecules Structure, Reactivity, Synthesis, and Applications," VCH, Weinheim (1988).
-
(1988)
Fluorine-Containing Molecules Structure, Reactivity, Synthesis, and Applications
-
-
Liebman, J.F.1
Greenberg, A.2
Dolbier Jr., W.R.3
-
11
-
-
0000829582
-
-
ed by H. Kropf, Thieme, Stuttgart
-
K.-P. Zeller, in "Houben-Weyl: Methoden der organischen Chemie," ed by H. Kropf, Thieme, Stuttgart (1985), Vol. 5/2C, pp. 127 - 418.
-
(1985)
Houben-Weyl: Methoden der Organischen Chemie
, vol.5
, Issue.2 C
, pp. 127-418
-
-
Zeller, K.-P.1
-
12
-
-
0006480892
-
-
H. J. Tobler, A. Bauder, and Hs. H. Günthard, J. Mol. Spectrosc., 18, 239 (1965).
-
(1965)
J. Mol. Spectrosc.
, vol.18
, pp. 239
-
-
Tobler, H.J.1
Bauder, A.2
Günthard, Hs.H.3
-
14
-
-
2742518456
-
-
By the CNDO/2 calculation: T. A. Holak, S. Sadigh-Esfandiary, F. R. Carter, and D. J. Sardella, J. Org. Chem., 45, 2400 (1980).
-
(1980)
J. Org. Chem.
, vol.45
, pp. 2400
-
-
Holak, T.A.1
Sadigh-Esfandiary, S.2
Carter, F.R.3
Sardella, D.J.4
-
15
-
-
0009032291
-
-
Antiulcer activities: H. Yamasaki, S. Irino, A. Uda, K. Uchida, H. Ohno, N. Saito, K. Kondo, K. Jinzenji, and T. Yamamoto, Nippon Yakurigaku Zasshi, 54, 362 (1958); S. Okabe, K. Takeuchi, K. Honda, and K. Takagi, Pharmacometrics, 9, 31 (1975); T. Yanagisawa, S. Wakabayashi, T. Tomiyama, M. Yasunami, and K. Takase, Chem. Pharm. Bull., 36, 641 (1988); S. Mochizuki, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Gastroenterol., 24 (Suppl. 162), 194 (1989).
-
(1958)
Nippon Yakurigaku Zasshi
, vol.54
, pp. 362
-
-
Yamasaki, H.1
Irino, S.2
Uda, A.3
Uchida, K.4
Ohno, H.5
Saito, N.6
Kondo, K.7
Jinzenji, K.8
Yamamoto, T.9
-
16
-
-
0016652266
-
-
Antiulcer activities: H. Yamasaki, S. Irino, A. Uda, K. Uchida, H. Ohno, N. Saito, K. Kondo, K. Jinzenji, and T. Yamamoto, Nippon Yakurigaku Zasshi, 54, 362 (1958); S. Okabe, K. Takeuchi, K. Honda, and K. Takagi, Pharmacometrics, 9, 31 (1975); T. Yanagisawa, S. Wakabayashi, T. Tomiyama, M. Yasunami, and K. Takase, Chem. Pharm. Bull., 36, 641 (1988); S. Mochizuki, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Gastroenterol., 24 (Suppl. 162), 194 (1989).
-
(1975)
Pharmacometrics
, vol.9
, pp. 31
-
-
Okabe, S.1
Takeuchi, K.2
Honda, K.3
Takagi, K.4
-
17
-
-
0023883194
-
-
Antiulcer activities: H. Yamasaki, S. Irino, A. Uda, K. Uchida, H. Ohno, N. Saito, K. Kondo, K. Jinzenji, and T. Yamamoto, Nippon Yakurigaku Zasshi, 54, 362 (1958); S. Okabe, K. Takeuchi, K. Honda, and K. Takagi, Pharmacometrics, 9, 31 (1975); T. Yanagisawa, S. Wakabayashi, T. Tomiyama, M. Yasunami, and K. Takase, Chem. Pharm. Bull., 36, 641 (1988); S. Mochizuki, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Gastroenterol., 24 (Suppl. 162), 194 (1989).
-
(1988)
Chem. Pharm. Bull.
, vol.36
, pp. 641
-
-
Yanagisawa, T.1
Wakabayashi, S.2
Tomiyama, T.3
Yasunami, M.4
Takase, K.5
-
18
-
-
0024430325
-
-
Antiulcer activities: H. Yamasaki, S. Irino, A. Uda, K. Uchida, H. Ohno, N. Saito, K. Kondo, K. Jinzenji, and T. Yamamoto, Nippon Yakurigaku Zasshi, 54, 362 (1958); S. Okabe, K. Takeuchi, K. Honda, and K. Takagi, Pharmacometrics, 9, 31 (1975); T. Yanagisawa, S. Wakabayashi, T. Tomiyama, M. Yasunami, and K. Takase, Chem. Pharm. Bull., 36, 641 (1988); S. Mochizuki, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Gastroenterol., 24 (Suppl. 162), 194 (1989).
-
(1989)
J. Gastroenterol.
, vol.24
, Issue.162 SUPPL.
, pp. 194
-
-
Mochizuki, S.1
Wakabayashi, S.2
Kosakai, K.3
Yokota, M.4
-
19
-
-
0025051239
-
-
2 antagonistic activities: T. Tomiyama, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Med. Chem., 33, 2323 (1990); T. Tomiyama, M. Yokota, S. Wakabayashi, K. Kosakai, and T. Yanagisawa, J. Med. Chem., 36, 791 (1993).
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2323
-
-
Tomiyama, T.1
Wakabayashi, S.2
Kosakai, K.3
Yokota, M.4
-
20
-
-
0027478776
-
-
2 antagonistic activities: T. Tomiyama, S. Wakabayashi, K. Kosakai, and M. Yokota, J. Med. Chem., 33, 2323 (1990); T. Tomiyama, M. Yokota, S. Wakabayashi, K. Kosakai, and T. Yanagisawa, J. Med. Chem., 36, 791 (1993).
-
(1993)
J. Med. Chem.
, vol.36
, pp. 791
-
-
Tomiyama, T.1
Yokota, M.2
Wakabayashi, S.3
Kosakai, K.4
Yanagisawa, T.5
-
21
-
-
0013119115
-
-
Retinoids: K. Nakanishi, F. Derguini, V. J. Rao, G. Zarrilli, M. Okabe, T. Lien, R. Johnson, K. W. Foster, and J. Saranak, Pure Appl. Chem., 61, 361 (1989); A. E. Asato, X.-Y. Li, D. Mead, G. M. L. Patterson, and R. S. H. Liu, J. Am. Chem. Soc., 112, 7398 (1990); A. E. Asato, A. Peng, M. Z. Hossain, T. Mirzadegan, and J. S. Bertram, J. Med. Chem., 36, 3137 (1993).
-
(1989)
Pure Appl. Chem.
, vol.61
, pp. 361
-
-
Nakanishi, K.1
Derguini, F.2
Rao, V.J.3
Zarrilli, G.4
Okabe, M.5
Lien, T.6
Johnson, R.7
Foster, K.W.8
Saranak, J.9
-
22
-
-
0025027787
-
-
Retinoids: K. Nakanishi, F. Derguini, V. J. Rao, G. Zarrilli, M. Okabe, T. Lien, R. Johnson, K. W. Foster, and J. Saranak, Pure Appl. Chem., 61, 361 (1989); A. E. Asato, X.-Y. Li, D. Mead, G. M. L. Patterson, and R. S. H. Liu, J. Am. Chem. Soc., 112, 7398 (1990); A. E. Asato, A. Peng, M. Z. Hossain, T. Mirzadegan, and J. S. Bertram, J. Med. Chem., 36, 3137 (1993).
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 7398
-
-
Asato, A.E.1
Li, X.-Y.2
Mead, D.3
Patterson, G.M.L.4
Liu, R.S.H.5
-
23
-
-
0027431354
-
-
Retinoids: K. Nakanishi, F. Derguini, V. J. Rao, G. Zarrilli, M. Okabe, T. Lien, R. Johnson, K. W. Foster, and J. Saranak, Pure Appl. Chem., 61, 361 (1989); A. E. Asato, X.-Y. Li, D. Mead, G. M. L. Patterson, and R. S. H. Liu, J. Am. Chem. Soc., 112, 7398 (1990); A. E. Asato, A. Peng, M. Z. Hossain, T. Mirzadegan, and J. S. Bertram, J. Med. Chem., 36, 3137 (1993).
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3137
-
-
Asato, A.E.1
Peng, A.2
Hossain, M.Z.3
Mirzadegan, T.4
Bertram, J.S.5
-
24
-
-
0040085934
-
-
Squarylium dyes: W. Ziegenbein and H.-E. Sprenger, Angew. Chem., 78, 937 (1966); P. M. Kazmaier, G. K. Hamer, and R. A. Burt, Can. J. Chem., 68, 530 (1990).
-
(1966)
Angew. Chem.
, vol.78
, pp. 937
-
-
Ziegenbein, W.1
Sprenger, H.-E.2
-
25
-
-
0006154967
-
-
Squarylium dyes: W. Ziegenbein and H.-E. Sprenger, Angew. Chem., 78, 937 (1966); P. M. Kazmaier, G. K. Hamer, and R. A. Burt, Can. J. Chem., 68, 530 (1990).
-
(1990)
Can. J. Chem.
, vol.68
, pp. 530
-
-
Kazmaier, P.M.1
Hamer, G.K.2
Burt, R.A.3
-
29
-
-
0001361724
-
-
b) T. Umemoto, K. Kawada, and K. Tomita, Tetrahedron Lett., 27, 4465 (1986);
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4465
-
-
Umemoto, T.1
Kawada, K.2
Tomita, K.3
-
30
-
-
0000601660
-
-
c) T. Umemoto, S. Fukami, G. Tomizawa, K. Harasawa, K. Kawada, and K. Tomita, J. Am. Chem. Soc., 112, 8563 (1990);
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 8563
-
-
Umemoto, T.1
Fukami, S.2
Tomizawa, G.3
Harasawa, K.4
Kawada, K.5
Tomita, K.6
-
31
-
-
0000950078
-
-
T. Umemoto, K. Harasawa, G. Tomizawa, K. Kawada, and K. Tomita, Bull. Chem. Soc. Jpn., 64, 1081 (1991).
-
(1991)
Bull. Chem. Soc. Jpn.
, vol.64
, pp. 1081
-
-
Umemoto, T.1
Harasawa, K.2
Tomizawa, G.3
Kawada, K.4
Tomita, K.5
-
32
-
-
0001590298
-
-
M. Yasunami, S, Miyoshi, N. Kanegae, and K. Takase, Bull. Chem. Soc. Jpn., 66, 892 (1993).
-
(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 892
-
-
Yasunami, M.1
Miyoshi, S.2
Kanegae, N.3
Takase, K.4
-
34
-
-
0000559438
-
-
K. Ziegler and K. Hafner, Angew. Chem., 67, 310 (1955); K. Hafner, Angew. Chem., 67, 301 (1955); K. Hafner, Justus Liebigs Ann. Chem., 606, 79 (1957); K. Hafner and H. Kaiser, Justus Liebigs Ann. Chem., 618, 140 (1958).
-
(1955)
Angew. Chem.
, vol.67
, pp. 310
-
-
Ziegler, K.1
Hafner, K.2
-
35
-
-
0004536053
-
-
K. Ziegler and K. Hafner, Angew. Chem., 67, 310 (1955); K. Hafner, Angew. Chem., 67, 301 (1955); K. Hafner, Justus Liebigs Ann. Chem., 606, 79 (1957); K. Hafner and H. Kaiser, Justus Liebigs Ann. Chem., 618, 140 (1958).
-
(1955)
Angew. Chem.
, vol.67
, pp. 301
-
-
Hafner, K.1
-
36
-
-
84982061643
-
-
K. Ziegler and K. Hafner, Angew. Chem., 67, 310 (1955); K. Hafner, Angew. Chem., 67, 301 (1955); K. Hafner, Justus Liebigs Ann. Chem., 606, 79 (1957); K. Hafner and H. Kaiser, Justus Liebigs Ann. Chem., 618, 140 (1958).
-
(1957)
Justus Liebigs Ann. Chem.
, vol.606
, pp. 79
-
-
Hafner, K.1
-
37
-
-
84982062272
-
-
K. Ziegler and K. Hafner, Angew. Chem., 67, 310 (1955); K. Hafner, Angew. Chem., 67, 301 (1955); K. Hafner, Justus Liebigs Ann. Chem., 606, 79 (1957); K. Hafner and H. Kaiser, Justus Liebigs Ann. Chem., 618, 140 (1958).
-
(1958)
Justus Liebigs Ann. Chem.
, vol.618
, pp. 140
-
-
Hafner, K.1
Kaiser, H.2
-
39
-
-
85033811343
-
-
note
-
1) the reaction mixture was poured into water to remove the resulting pyridinium salts as described in Ref. 21 and the products were extracted with benzene, however, extraction with hydrocarbon solvent was difficult due to the formation of a large amount of precipitates. In this paper, therefore, the results without the aqueous workup were described (see Experimental).
-
-
-
-
42
-
-
37049067287
-
-
T. M. Bockman, K. Y. Lee, and J. K. Kochi, J. Chem. Soc., Perkin Trans. 2, 1992, 1581.
-
(1581)
J. Chem. Soc., Perkin Trans.
, vol.2
, pp. 1992
-
-
Bockman, T.M.1
Lee, K.Y.2
Kochi, J.K.3
-
43
-
-
84982065370
-
-
(1-Azulenyl)pyridines have not been reported so far. Cf. 2-(4-Azulenylpyridine: K. Hafner, C. Bernhard, and R. Müller, Justus Liebigs Ann. Chem., 650, 35 (1961);
-
(1961)
Justus Liebigs Ann. Chem.
, vol.650
, pp. 35
-
-
Hafner, K.1
Bernhard, C.2
Müller, R.3
-
45
-
-
85033814989
-
-
note
-
When a more powerful reagent, 2,6-dichloro-N-fluoropyridinium tetrafluoroborate, was used, no azulenylpyridines were obtained. The characterization of the resulting CT-complex is in progress.
-
-
-
-
46
-
-
0343518747
-
-
A. G. Anderson, Jr., and J. J.Tazuma, J. Am. Chem. Soc., 75, 4979 (1953); A. G. Anderson, Jr., J. A. Nelson, and J. J. Tazuma, J. Am. Chem. Soc., 75, 4980 (1953).
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 4979
-
-
Anderson Jr., A.G.1
Tazuma, J.J.2
-
47
-
-
0000448759
-
-
A. G. Anderson, Jr., and J. J.Tazuma, J. Am. Chem. Soc., 75, 4979 (1953); A. G. Anderson, Jr., J. A. Nelson, and J. J. Tazuma, J. Am. Chem. Soc., 75, 4980 (1953).
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 4980
-
-
Anderson, A.G.1
Jr2
Nelson, J.A.3
Tazuma, J.J.4
-
48
-
-
0001070042
-
-
R. N. McDonald, H. E. Petty, N. L. Wolfe, and J. V. Paukstelis, J. Ong. Chem., 39, 1877 (1974); T. Nozoe, P.-W. Yang, C.-P. Wu, T-S. Huang, T-H. Lee, H. Okai, H. Wakabayashi, and S. Ishikawa, Heterocycles, 29, 1225 (1989).
-
(1974)
J. Ong. Chem.
, vol.39
, pp. 1877
-
-
McDonald, R.N.1
Petty, H.E.2
Wolfe, N.L.3
Paukstelis, J.V.4
-
49
-
-
0000215512
-
-
R. N. McDonald, H. E. Petty, N. L. Wolfe, and J. V. Paukstelis, J. Ong. Chem., 39, 1877 (1974); T. Nozoe, P.-W. Yang, C.-P. Wu, T-S. Huang, T-H. Lee, H. Okai, H. Wakabayashi, and S. Ishikawa, Heterocycles, 29, 1225 (1989).
-
(1989)
Heterocycles
, vol.29
, pp. 1225
-
-
Nozoe, T.1
Yang, P.-W.2
Wu, C.-P.3
Huang, T.-S.4
Lee, T.-H.5
Okai, H.6
Wakabayashi, H.7
Ishikawa, S.8
-
50
-
-
84988130722
-
-
E. Differding and H. Ofner, Synlett, 1991, 187; E. Differding, R. O. Duthaler, A. Krieger, G. M. Rüegg, and C. Schmit, Synlett, 1991, 395.
-
(1991)
Synlett
, pp. 187
-
-
Differding, E.1
Ofner, H.2
-
51
-
-
85033821017
-
-
E. Differding and H. Ofner, Synlett, 1991, 187; E. Differding, R. O. Duthaler, A. Krieger, G. M. Rüegg, and C. Schmit, Synlett, 1991, 395.
-
(1991)
Synlett
, pp. 395
-
-
Differding, E.1
Duthaler, R.O.2
Krieger, A.3
Rüegg, G.M.4
Schmit, C.5
-
52
-
-
37049071468
-
-
R. E. Banks, S. N. Mohialdin-Khaffaf, G. S. Lal, I. Sharif, and R. G. Syvret, J. Chem. Soc., Chem. Commun., 1992, 595; G. S. Lal, J. Org. Chem., 58, 2791 (1993).
-
J. Chem. Soc., Chem. Commun.
, vol.1992
, pp. 595
-
-
Banks, R.E.1
Mohialdin-Khaffaf, S.N.2
Lal, G.S.3
Sharif, I.4
Syvret, R.G.5
-
53
-
-
0000815463
-
-
R. E. Banks, S. N. Mohialdin-Khaffaf, G. S. Lal, I. Sharif, and R. G. Syvret, J. Chem. Soc., Chem. Commun., 1992, 595; G. S. Lal, J. Org. Chem., 58, 2791 (1993).
-
(1993)
J. Org. Chem.
, vol.58
, pp. 2791
-
-
Lal, G.S.1
-
54
-
-
0029118869
-
-
S. Stavber, M. Zupan, A. J. Poss, and G. A. Shia, Tetrahedron Lett., 36, 6769 (1995).
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 6769
-
-
Stavber, S.1
Zupan, M.2
Poss, A.J.3
Shia, G.A.4
-
58
-
-
28944450366
-
-
W. Treibs, H.-J. Neupert, and J. Hiebsch, Chem. Ber., 92, 141 (1959).
-
(1959)
Chem. Ber.
, vol.92
, pp. 141
-
-
Treibs, W.1
Neupert, H.-J.2
Hiebsch, J.3
-
59
-
-
85033822129
-
-
submitted
-
4 follwed by the usual aqueous workup gave 1-phenylazulene (1d) in 88% yield: M. Yasunami, M. Kurita, T. Ueno, S. Miyoshi, M. Sato, T. Tomofuji, M. Yoshifuji, and K. Takase, Heterocycles, submitted.
-
Heterocycles
-
-
Yasunami, M.1
Kurita, M.2
Ueno, T.3
Miyoshi, S.4
Sato, M.5
Tomofuji, T.6
Yoshifuji, M.7
Takase, K.8
-
61
-
-
0002191374
-
-
M. Yasunami, A. Chen, P. W. Yang, and K. Takase, Chem. Lett., 1980, 579.
-
Chem. Lett.
, vol.1980
, pp. 579
-
-
Yasunami, M.1
Chen, A.2
Yang, P.W.3
Takase, K.4
-
63
-
-
0011198729
-
-
Pl. A. Plattner, A. Fürst, M. Gordon, and K. Zimmermann, Helv. Chim. Acta, 33, 1910 (1950).
-
(1950)
Helv. Chim. Acta
, vol.33
, pp. 1910
-
-
Plattner, P.A.1
Fürst, A.2
Gordon, M.3
Zimmermann, K.4
-
66
-
-
4243462636
-
-
Jpn. Kokai Tokkyo Koho JP 62-207232
-
M. Yasunami and K. Takase, Jpn. Kokai Tokkyo Koho JP 62-207232; Chem. Abstr., 108, 221338s (1988).
-
(1988)
Chem. Abstr.
, vol.108
-
-
Yasunami, M.1
Takase, K.2
-
67
-
-
0342786899
-
-
T. M. Jacob, P. A. Vatakencherry, and S. Dev, Tetrahedron, 20, 2815 (1964).
-
(1964)
Tetrahedron
, vol.20
, pp. 2815
-
-
Jacob, T.M.1
Vatakencherry, P.A.2
Dev, S.3
-
68
-
-
85033822530
-
-
submitted
-
4 followed by the usual aqueous workup gave 2-phenylazulene (11b) in 92% yield: M. Yasunami, T. Ueno, Y. Kawai, I. Awaka, M. Yoshifuji, and K. Takase, Synthesis, submitted.
-
Synthesis
-
-
Yasunami, M.1
Ueno, T.2
Kawai, Y.3
Awaka, I.4
Yoshifuji, M.5
Takase, K.6
-
69
-
-
0011203490
-
-
Pl. A. Plattner, R. Sandrin, and J. Wyss, Helv. Chim. Acta, 29, 1604 (1946).
-
(1946)
Helv. Chim. Acta
, vol.29
, pp. 1604
-
-
Plattner, Pl.A.1
Sandrin, R.2
Wyss, J.3
-
70
-
-
2742522803
-
-
Y. N. Porshnev, E. M. Tereshchenko, and V. A. Churkina, Zh. Org. Khim., 10, 881 (1974); Chem. Abstr., 81, 25306q (1974).
-
(1974)
Zh. Org. Khim.
, vol.10
, pp. 881
-
-
Porshnev, Y.N.1
Tereshchenko, E.M.2
Churkina, V.A.3
-
71
-
-
85033817656
-
-
Y. N. Porshnev, E. M. Tereshchenko, and V. A. Churkina, Zh. Org. Khim., 10, 881 (1974); Chem. Abstr., 81, 25306q (1974).
-
(1974)
Chem. Abstr.
, vol.81
-
-
-
73
-
-
0001849749
-
-
The steric effect of 2-substituents on the CT-complex formation was also observed on the DDQ oxidation of 1-alkylazulenes. The oxidation of methyl 3-methylazulene-1-carboxylate with 2.2 equivalents of DDQ in aqueous acetone at room temperature for 30 min gave the 3-formyl derivative in 82% yield without recovery, however, methyl 3-methyl-2-phenylazulene-1-carboxylate was oxidized with 5 equivalents of DDQ for 4 h to give the 3-formyl derivative in 79% yield together with 12% of recovery. Cf. T. Amemiya, M. Yasunami, and K. Takase, Chem. Lett., 1977, 587.
-
(1977)
Chem. Lett.
, pp. 587
-
-
Amemiya, T.1
Yasunami, M.2
Takase, K.3
-
74
-
-
0001168749
-
-
S. Singh, D. D. DesMarteau, S. S. Zuberi, M. Witz, and H.-N. Huang, J. Am. Chem. Soc., 109, 7194 (1987).
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 7194
-
-
Singh, S.1
Desmarteau, D.D.2
Zuberi, S.S.3
Witz, M.4
Huang, H.-N.5
-
77
-
-
85033827067
-
-
note
-
-1 H coupling constants, although, the structure of "7-chloro-1-fluoroazulene" should be reconsidered.
-
-
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-
78
-
-
85033821366
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-
note
-
On the basis of the FT-IR spectroscopic data, the streching frequencies of the azulene skeleton of 1,3-difluoroazulenes appeared at longer regions than those of azulene and 1-fluoroazulenes.
-
-
-
-
79
-
-
37049109620
-
-
D. Doddrell, M. Barfield, W. Adcock, M. Aurangzeb, and D. Jordan, J. Chem. Soc., Perkin Trans. 2, 1976, 402. See also: P. R. Wells and D. Doddrell, J. Chem. Soc., Perkin Trans. 2, 1974, 1745; W. Kitching, M. Bullpitt, D. Gartshore, W. Adcock, T. C. Khor, D. Doddrell, and I. D. Rae, J. Org. Chem., 42, 2411 (1977).
-
(1976)
J. Chem. Soc., Perkin Trans.
, vol.2
, pp. 402
-
-
Doddrell, D.1
Barfield, M.2
Adcock, W.3
Aurangzeb, M.4
Jordan, D.5
-
80
-
-
37049114552
-
-
D. Doddrell, M. Barfield, W. Adcock, M. Aurangzeb, and D. Jordan, J. Chem. Soc., Perkin Trans. 2, 1976, 402. See also: P. R. Wells and D. Doddrell, J. Chem. Soc., Perkin Trans. 2, 1974, 1745; W. Kitching, M. Bullpitt, D. Gartshore, W. Adcock, T. C. Khor, D. Doddrell, and I. D. Rae, J. Org. Chem., 42, 2411 (1977).
-
(1974)
J. Chem. Soc., Perkin Trans. 2
, pp. 1745
-
-
Wells, P.R.1
Doddrell, D.2
-
81
-
-
0001613999
-
-
D. Doddrell, M. Barfield, W. Adcock, M. Aurangzeb, and D. Jordan, J. Chem. Soc., Perkin Trans. 2, 1976, 402. See also: P. R. Wells and D. Doddrell, J. Chem. Soc., Perkin Trans. 2, 1974, 1745; W. Kitching, M. Bullpitt, D. Gartshore, W. Adcock, T. C. Khor, D. Doddrell, and I. D. Rae, J. Org. Chem., 42, 2411 (1977).
-
(1977)
J. Org. Chem.
, vol.42
, pp. 2411
-
-
Kitching, W.1
Bullpitt, M.2
Gartshore, D.3
Adcock, W.4
Khor, T.C.5
Doddrell, D.6
Rae, I.D.7
-
82
-
-
37049076643
-
-
E. V. Dehmlow, D. Balschukat, P. P. Schmidt, and R. Krause, J. Chem. Soc., Chem. Commun., 1986, 1435.
-
(1986)
J. Chem. Soc., Chem. Commun.
, pp. 1435
-
-
Dehmlow, E.V.1
Balschukat, D.2
Schmidt, P.P.3
Krause, R.4
-
83
-
-
84970554519
-
-
P. R. Wells, K. G. Penman, and I. D. Rae, Aust. J. Chem., 33, 2221 (1980).
-
(1980)
Aust. J. Chem.
, vol.33
, pp. 2221
-
-
Wells, P.R.1
Penman, K.G.2
Rae, I.D.3
-
84
-
-
84982337304
-
-
Electron-donating groups on the odd-numbered positions are bathochromic and electron-withdrawing groups are hypsochromic. Pl. A. Plattner, Helv. Chim. Acta, 24, 283E (1941); Pl. A. Plattner and E. Heilbronner, Helv. Chim, Acta, 30, 910 (1947); Pl. A. Plattner, A. Fürst, and K. Jirasek, Helv. Chim. Acta, 30, 1320 (1947).
-
(1941)
Helv. Chim. Acta
, vol.24
-
-
Plattner, Pl.A.1
-
85
-
-
0042690789
-
-
Electron-donating groups on the odd-numbered positions are bathochromic and electron-withdrawing groups are hypsochromic. Pl. A. Plattner, Helv. Chim. Acta, 24, 283E (1941); Pl. A. Plattner and E. Heilbronner, Helv. Chim, Acta, 30, 910 (1947); Pl. A. Plattner, A. Fürst, and K. Jirasek, Helv. Chim. Acta, 30, 1320 (1947).
-
(1947)
Helv. Chim, Acta
, vol.30
, pp. 910
-
-
Plattner, Pl.A.1
Heilbronner, E.2
-
86
-
-
2742586503
-
-
Electron-donating groups on the odd-numbered positions are bathochromic and electron-withdrawing groups are hypsochromic. Pl. A. Plattner, Helv. Chim. Acta, 24, 283E (1941); Pl. A. Plattner and E. Heilbronner, Helv. Chim, Acta, 30, 910 (1947); Pl. A. Plattner, A. Fürst, and K. Jirasek, Helv. Chim. Acta, 30, 1320 (1947).
-
(1947)
Helv. Chim. Acta
, vol.30
, pp. 1320
-
-
Plattner, Pl.A.1
Fürst, A.2
Jirasek, K.3
-
92
-
-
0000383437
-
-
R. Boothe, C. Dial, R. Conaway, R. M. Pagni, and G. W. Kabalka, Tetrahedron Lett., 27, 2207 (1986).
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 2207
-
-
Boothe, R.1
Dial, C.2
Conaway, R.3
Pagni, R.M.4
Kabalka, G.W.5
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