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1
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0345125590
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Present address: Biomolecular Engineering Research Institute, Suita 565
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Present address: Biomolecular Engineering Research Institute, Suita 565.
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2
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1542502091
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For recent reviews, see: (a) Yasumoto T.; Murata, M. Chem, Rev. 1993, 93, 1897.
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(1993)
Chem, Rev.
, vol.93
, pp. 1897
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Yasumoto, T.1
Murata, M.2
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4
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0024815125
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Relative structure: (a) Murata, M.; Legrand, A. M.; Ishibashi, Y.; Yasumoto, T. J. Am. Chem. Soc. 1989, 111, 8929.
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(1989)
J. Am. Chem. Soc.
, vol.111
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Murata, M.1
Legrand, A.M.2
Ishibashi, Y.3
Yasumoto, T.4
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5
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0025045174
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(b) Murata, M.; Legrand, A. M.; Ishibashi, Y.; Fukui, M.; Yasumoto, T. ibid. 1990, 112, 4380.
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(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4380
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Murata, M.1
Legrand, A.M.2
Ishibashi, Y.3
Fukui, M.4
Yasumoto, T.5
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6
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0030670907
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Absolute configuration: (a) Satake, M.; Morohashi, A.; Oguri, H.; Oishi, T.; Hirama, M.; Harada, N.; Yasumoto, T. J. Am. Chem. Soc. 1997, 119, 11325.
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(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 11325
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Satake, M.1
Morohashi, A.2
Oguri, H.3
Oishi, T.4
Hirama, M.5
Harada, N.6
Yasumoto, T.7
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7
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0031550831
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(b) Oguri, H.; Hishiyama, S.; Sato, O.; Oishi, T.; Hirama, M.; Murata, M.; Yasumoto, T.; Harada, N. Tetrahedron 1997, 53, 3057.
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(1997)
Tetrahedron
, vol.53
, pp. 3057
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Oguri, H.1
Hishiyama, S.2
Sato, O.3
Oishi, T.4
Hirama, M.5
Murata, M.6
Yasumoto, T.7
Harada, N.8
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8
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0029263484
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Yasumoto, T.; Fukui, M.; Sasaki, K.; Sugiyama, K. J. A. O. A. C. Intern. 1995, 78, 574.
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(1995)
J. A. O. A. C. Intern.
, vol.78
, pp. 574
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Yasumoto, T.1
Fukui, M.2
Sasaki, K.3
Sugiyama, K.4
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9
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0022389585
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(a) Hokama Y. Toxicon 1985, 23, 939.
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(1985)
Toxicon
, vol.23
, pp. 939
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Hokama, Y.1
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11
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0345557088
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in press
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Production of mAbs to the synthetic JKLM-ring fragment-carrier protein conjugates has been reported by K. Tachibana and co-workers, see: Pauillac, S.; Inoue, M.; Sasaki, M.; Naar, J.; Murata, M.; Tachibana, K.; Chinain, M.; Legrand, A. M. Eur. J. Ichthyol., in press.
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Eur. J. Ichthyol.
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Pauillac, S.1
Inoue, M.2
Sasaki, M.3
Naar, J.4
Murata, M.5
Tachibana, K.6
Chinain, M.7
Legrand, A.M.8
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12
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0003060427
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and Ref. 4b
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Oguri, H.; Hishiyama, S.; Oishi, T.; Hirama, M. Synlett 1996, 1252, and Ref. 4b.
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(1996)
Synlett
, pp. 1252
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Oguri, H.1
Hishiyama, S.2
Oishi, T.3
Hirama, M.4
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13
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0033534666
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For other synthetic studies of the ABC-ring fragment, see: (a) Hosokawa, S.; Isobe, M. J. Org. Chem. 1999, 64, 37.
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(1999)
J. Org. Chem.
, vol.64
, pp. 37
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Hosokawa, S.1
Isobe, M.2
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14
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0002320739
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(b) Oka, T.; Fujiwara, K.; Murai, A. Tetrahedron 1998, 38, 21.
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(1998)
Tetrahedron
, vol.38
, pp. 21
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Oka, T.1
Fujiwara, K.2
Murai, A.3
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16
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85045568522
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(a) Horita, K.; Hachiya, S.; Nagasawa, M.; Hikota, M.; Yonemitsu, O. Synlett 1994, 38.
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(1994)
Synlett
, pp. 38
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Horita, K.1
Hachiya, S.2
Nagasawa, M.3
Hikota, M.4
Yonemitsu, O.5
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17
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0028010945
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(b) Burke, S. D.; Jung, K. W.; Phillips, J. R.; Perri, R.E. Tetrahedron Lett. 1994, 35, 703.
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(1994)
Tetrahedron Lett.
, vol.35
, pp. 703
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Burke, S.D.1
Jung, K.W.2
Phillips, J.R.3
Perri, R.E.4
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18
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0032572856
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(c) Kadota, I.; Park, C.-H.; Ohtaka, M.; Oguro, N.; Yamamoto, Y, Tetrahedron Lett. 1998, 39, 6365.
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 6365
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Kadota, I.1
Park, C.-H.2
Ohtaka, M.3
Oguro, N.4
Yamamoto, Y.5
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19
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0345557085
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The carbon numbering corresponding to that of CTX1B has been used throughout this paper
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The carbon numbering corresponding to that of CTX1B has been used throughout this paper.
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20
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0015406165
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Kitagawa, T.; Miura, T.; Tanimiya, H. Chem. Pharm. Bull. 1972, 20, 2176.
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(1972)
Chem. Pharm. Bull.
, vol.20
, pp. 2176
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Kitagawa, T.1
Miura, T.2
Tanimiya, H.3
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22
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0344694880
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IgG subclass of 4H2, 6F12 and 6H7 was determined as IgG1λ, IgG3κ and IgG1κ, respectively
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IgG subclass of 4H2, 6F12 and 6H7 was determined as IgG1λ, IgG3κ and IgG1κ, respectively.
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23
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0345557087
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The 2,11-bis-p-bromobenzoates, 27 and 28, were converted to the 1,2,11-tris-p-bromobenzoates, 29 and 30, which showed the characteristic CD spectra as reported previously. Assignment of the C2 configuration by CD spectra of the tris-p-bromobenzoates is described in Ref 8
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The 2,11-bis-p-bromobenzoates, 27 and 28, were converted to the 1,2,11-tris-p-bromobenzoates, 29 and 30, which showed the characteristic CD spectra as reported previously. Assignment of the C2 configuration by CD spectra of the tris-p-bromobenzoates is described in Ref 8.
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24
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85087235412
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ext = 253 nm (Δε+19.4), 236 nm (-4.6)
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ext = 253 nm (Δε+19.4), 236 nm (-4.6).
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