-
1
-
-
0028213668
-
-
For total syntheses of taxol, see: a) R. A. Holton, C. Somoza, H.-B. Kim, F. Liang, R. J. Biediger, P. D. Boatman, M. Shindo, C. C. Smith, S. Kim, H. Nadizadeh, Y. Suzuki, C. Tao, P. Vu, S. Tang, P. Zhang, K. K. Murthi, L. N. Gentile, and J. H. Liu, J. Am. Chem. Soc., 116, 1597, (1994); R. A. Holton, H.-B. Kim, C. Somoza, F. Liang, R. J. Biediger, P. D. Boatman, M. Shindo, C. C. Smith, S. Kim, H. Nadizadeh, Y, Suzuki, C. Tao, P. Vu, S. Tang, P. Zhang, K. K. Murthi, L. N. Gentile, and J. H. Liu, J. Am. Chem. Soc., 116, 1599 (1994);
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 1597
-
-
Holton, R.A.1
Somoza, C.2
Kim, H.-B.3
Liang, F.4
Biediger, R.J.5
Boatman, P.D.6
Shindo, M.7
Smith, C.C.8
Kim, S.9
Nadizadeh, H.10
Suzuki, Y.11
Tao, C.12
Vu, P.13
Tang, S.14
Zhang, P.15
Murthi, K.K.16
Gentile, L.N.17
Liu, J.H.18
-
2
-
-
0028353983
-
-
For total syntheses of taxol, see: a) R. A. Holton, C. Somoza, H.-B. Kim, F. Liang, R. J. Biediger, P. D. Boatman, M. Shindo, C. C. Smith, S. Kim, H. Nadizadeh, Y. Suzuki, C. Tao, P. Vu, S. Tang, P. Zhang, K. K. Murthi, L. N. Gentile, and J. H. Liu, J. Am. Chem. Soc., 116, 1597, (1994); R. A. Holton, H.-B. Kim, C. Somoza, F. Liang, R. J. Biediger, P. D. Boatman, M. Shindo, C. C. Smith, S. Kim, H. Nadizadeh, Y, Suzuki, C. Tao, P. Vu, S. Tang, P. Zhang, K. K. Murthi, L. N. Gentile, and J. H. Liu, J. Am. Chem. Soc., 116, 1599 (1994);
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 1599
-
-
Holton, R.A.1
Kim, H.-B.2
Somoza, C.3
Liang, F.4
Biediger, R.J.5
Boatman, P.D.6
Shindo, M.7
Smith, C.C.8
Kim, S.9
Nadizadeh, H.10
Suzuki, Y.11
Tao, C.12
Vu, P.13
Tang, S.14
Zhang, P.15
Murthi, K.K.16
Gentile, L.N.17
Liu, J.H.18
-
3
-
-
0028012837
-
-
b) K. C. Nicolaou, Z. Yang, J. J. Liu, H. Ueno, P. G. Nantermet, R. K. Guy, C. F. Claiborne, J. Renaud, E. A. Couladouros, K. Paulvannan, and E. J. Sorensen, Nature, 367, 630 (1994);
-
(1994)
Nature
, vol.367
, pp. 630
-
-
Nicolaou, K.C.1
Yang, Z.2
Liu, J.J.3
Ueno, H.4
Nantermet, P.G.5
Guy, R.K.6
Claiborne, C.F.7
Renaud, J.8
Couladouros, E.A.9
Paulvannan, K.10
Sorensen, E.J.11
-
4
-
-
33748237378
-
-
c) J. J. Masters, J. T. Link, L. B. Snyder, W. B. Young, and S. J. Danishefsky, Angew. Chem., Int. Ed. Engl., 34, 1723 (1995).
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 1723
-
-
Masters, J.J.1
Link, J.T.2
Snyder, L.B.3
Young, W.B.4
Danishefsky, S.J.5
-
5
-
-
0000883118
-
-
Synthesis of precursor of 8-membered ring compound; T. Mukaiyama, I. Shiina, K. Sakata, T. Emura, K. Seto, and M. Saitoh, Chem. Lett., 1995, 179.
-
Chem. Lett.
, vol.1995
, pp. 179
-
-
Mukaiyama, T.1
Shiina, I.2
Sakata, K.3
Emura, T.4
Seto, K.5
Saitoh, M.6
-
6
-
-
0002885009
-
-
Synthesis of optically active 8-membered ring compound; I. Shiina, K. Uoto, N. Mori, T. Kosugi, and T. Mukaiyama, Chem. Lett., 1995, 181.
-
Chem. Lett.
, vol.1995
, pp. 181
-
-
Shiina, I.1
Uoto, K.2
Mori, N.3
Kosugi, T.4
Mukaiyama, T.5
-
7
-
-
0002540237
-
-
Synthesis of AB ring model system; T. Mukaiyama, I. Shiina, K. Kimura, Y. Akiyama, and H. Iwadare, Chem. Lett., 1995, 229.
-
Chem. Lett.
, vol.1995
, pp. 229
-
-
Mukaiyama, T.1
Shiina, I.2
Kimura, K.3
Akiyama, Y.4
Iwadare, H.5
-
8
-
-
0002819992
-
-
Synthesis of optically active AB ring system; I. Shiina, H. Iwadare, M. Saitoh, N. Ohkawa, T. Nishimura, and T. Mukaiyama, Chem. Lett., 1995, 781.
-
Chem. Lett.
, vol.1995
, pp. 781
-
-
Shiina, I.1
Iwadare, H.2
Saitoh, M.3
Ohkawa, N.4
Nishimura, T.5
Mukaiyama, T.6
-
9
-
-
0030489318
-
-
Synthesis of optically active BC ring system; T. Mukaiyama, I. Shiina, H. Iwadare, M. Saitoh, K. Nishimura, T. Nishimura, N. Ohkawa, H. Sakoh, and K. Saitoh, Chem. Lett., 1996, 483.
-
Chem. Lett.
, vol.1996
, pp. 483
-
-
Mukaiyama, T.1
Shiina, I.2
Iwadare, H.3
Saitoh, M.4
Nishimura, K.5
Nishimura, T.6
Ohkawa, N.7
Sakoh, H.8
Saitoh, K.9
-
10
-
-
0001931392
-
-
Retrosynthetic and synthetic studies; I. Shiina, M. Saitoh, K. Nishimura, K. Saitoh, and T. Mukaiyama., Chem. Lett., 1996, 223.
-
Chem. Lett.
, vol.1996
, pp. 223
-
-
Shiina, I.1
Saitoh, M.2
Nishimura, K.3
Saitoh, K.4
Mukaiyama, T.5
-
11
-
-
0039435667
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note
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28 +31.1° (c 0.793, benzene).
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