Enantiospecific, Stereospecific Total Synthesis of the Oxindole Alkaloid Alstonisine

Organic Letters - Tập 4 Số 24 - Trang 4237-4240 - 2002
Xiangyu Z. Wearing1, James M. Cook1
1Department of Chemistry, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53201

Tóm tắt

Từ khóa


Tài liệu tham khảo

Elderfield R. C., 1972, Phytochemistry, 11, 339, 10.1016/S0031-9422(00)90012-8

Ghedira K., 1988, Phytochemistry, 27, 3955, 10.1016/0031-9422(88)83053-X

Wong W. H., 1996, Phytochemistry, 41, 313, 10.1016/0031-9422(96)81092-2

Nordman C. E., 1963, J. Am. Chem. Soc., 85, 353, 10.1021/ja00886a028

Garnick R. L., 1978, J. Am. Chem. Soc., 100, 4213, 10.1021/ja00481a034

Rahman A., 1987, Phytochemistry, 26, 865, 10.1016/S0031-9422(00)84811-6

Rahman A., 1988, Heterocycles, 27, 725, 10.3987/COM-87-4401

Yu P., 1997, Tetrahedron Lett., 38, 8799, 10.1016/S0040-4039(97)10420-8

Hollinshead S. P., 1989, Heterocycles, 29, 529, 10.3987/COM-89-4839

Peterson A. C., 1995, J. Org. Chem., 60, 120, 10.1021/jo00106a024

Bi Y., 1993, The Synthesis of Macroline Related Indole Alkaloids, 13

Hamaker, L. K.; Cook, J. M. InAlkaloids:Chemical and BiologicalPerspectives; Pelletier, S. W., Ed.; Elsevier Science:  New York, 1995; Vol. 9, p 23.

Wright C. W., 1992, Phytother. Res., 6, 121, 10.1002/ptr.2650060303

Mayerl F., 1978, Helv. Chim. Acta, 61, 337, 10.1002/hlca.19780610130

Harada M., 1978, Chem. Pharm. Bull, 26, 48, 10.1248/cpb.26.48

Sakai S., 1975, Chem. Pharm. Bull, 23, 48, 10.1248/cpb.23.2805

Silverton J. V., 1982, J. Chem. Soc., Perkin Trans., 1, 1263, 10.1039/p19820001263

Haginiwa J., 1970, Yakugaku Zasshi, 90, 219, 10.1248/yakushi1947.90.2_219

Sakai S., 1991, Chem. Abstr., 117, 97324

Yu P., 1998, J. Org. Chem., 63, 9160, 10.1021/jo981815h

Yu P., 2000, J. Org. Chem., 65, 3173, 10.1021/jo000126e

Niclaou K. C., 1979, J. Am. Chem. Soc., 101, 3704, 10.1021/ja00507a069

Takayama H., 1991, Tetrahedron, 47, 1383, 10.1016/S0040-4020(01)86414-0

Zhang L. H., 1990, J. Am. Chem. Soc., 112, 4088, 10.1021/ja00166a084

Fleming I., 1982, Tetrahedron Lett., 23, 2053, 10.1016/S0040-4039(00)87259-7

Yang C.-C., 1993, J. Org. Chem., 58, 3100, 10.1021/jo00063a032

Jones K., 1986, J. Chem. Soc., Chem. Commun., 115, 10.1039/C39860000115

Wright C. W., 1987, Tetrahedron Lett., 28, 6389, 10.1016/S0040-4039(01)91381-4

Jones K., 1989, Tetrahedron Lett., 2657, 10.1016/S0040-4039(00)99091-9

Jones K., 1992, J. Chem. Soc., Chem. Commun., 1766, 10.1039/c39920001766

Hart D. J., 1991, Tetrahedron Lett., 32, 4099, 10.1016/S0040-4039(00)79873-X

Clark A. J., 1994, J. Chem. Soc., Chem. Commun., 41, 10.1039/C39940000041

Dutton J. K., 1994, J. Chem. Soc., Chem. Commun., 765, 10.1039/c39940000765

Abelman M. M., 1987, J. Org. Chem., 52, 4130, 10.1021/jo00227a038

Early W. G., 1988, Tetrahedron Lett., 29, 3785, 10.1016/S0040-4039(00)82114-0

Almeida P. S., 1991, Tetrahedron Lett., 32, 2671, 10.1016/S0040-4039(00)78815-0

Madin A., 1992, Tetrahedron Lett., 33, 4859, 10.1016/S0040-4039(00)61217-0

Ashimori A., 1992, J. Org. Chem., 57, 4571, 10.1021/jo00043a005

Grigg R., 1993, Tetrahedron Lett., 34, 7471, 10.1016/S0040-4039(00)60156-9

Zang X., 1993, J. Am. Chem. Soc., 115, 8876, 10.1021/ja00055a076

Güller, R.; Borschberg, H.J.Tetrahedron:  Asymmetry1992,3, 1197.

Güller R., 1993, Helv. Chim. Acta, 76, 1847, 10.1002/hlca.19930760505

Güller R., 1994, Tetrahedron Lett., 35, 865, 10.1016/S0040-4039(00)75984-3

Fu X., 1993, J. Org. Chem., 58, 661, 10.1021/jo00055a019

Sakai S., 1982, J. Chem. Soc., Perkin Trans. 1, 12, 1257, 10.1039/p19820001257

Sakai S., 1975, Tetrahedron Lett., 10, 719, 10.1016/S0040-4039(00)71966-6

Fu X., 1992, J. Am. Chem. Soc., 114, 6910, 10.1021/ja00043a043

Esmond R. W., 1980, J. Am. Chem. Soc., 102, 7116, 10.1021/ja00543a045

Yu P. Ph.D., 1999, University of Wisconsin-Milwaukee

Zhang L. H., 1989, J. Am. Chem. Soc., 111, 8263, 10.1021/ja00203a030

Kam T. S., 2000, Tetrahedron, 56, 6143, 10.1016/S0040-4020(00)00564-0