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1
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0002085548
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For examples, see: a
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For examples, see: a) M. M. Midland, A. Tramontano, J. R. Cable, J. Org. Chem. 1980, 45, 28-29;
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(1980)
J. Org. Chem
, vol.45
, pp. 28-29
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Midland, M.M.1
Tramontano, A.2
Cable, J.R.3
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2
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0021510134
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b) R. Noyori, T. M. Yamada, M. Nishizawa, J. Am. Chem. Soc. 1984, 106, 6717-6725;
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(1984)
J. Am. Chem. Soc
, vol.106
, pp. 6717-6725
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Noyori, R.1
Yamada, T.M.2
Nishizawa, M.3
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3
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0027232023
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c) M.T. Crimmins, D. K. Jung, J.L. Gray, J. Am. Chem. Soc. 1993, 115, 3146-3155;
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(1993)
J. Am. Chem. Soc
, vol.115
, pp. 3146-3155
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Crimmins, M.T.1
Jung, D.K.2
Gray, J.L.3
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5
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0028911508
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e) H. Corlay, R. T. Lewis, W. B. Motherwell, M. Shipman, Tetrahedron 1995, 51, 3303-3318;
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(1995)
Tetrahedron
, vol.51
, pp. 3303-3318
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Corlay, H.1
Lewis, R.T.2
Motherwell, W.B.3
Shipman, M.4
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6
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0037204712
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G. A. Molander, D. J. St. Jean, J. Org. Chem. 2002, 67, 3861-3865;
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f) G. A. Molander, D. J. St. Jean, J. Org. Chem. 2002, 67, 3861-3865;
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7
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7444246242
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B. M. Trost, Z. T. Ball, J. Am. Chem. Soc. 2004, 126, 13942-13944;
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g) B. M. Trost, Z. T. Ball, J. Am. Chem. Soc. 2004, 126, 13942-13944;
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8
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33744801116
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B. G. Pujanauski, B. A. B. Prasad, R. Sarpong, J. Am. Chem. Soc. 2006, 128, 6786-6787;
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h) B. G. Pujanauski, B. A. B. Prasad, R. Sarpong, J. Am. Chem. Soc. 2006, 128, 6786-6787;
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-
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9
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58149278666
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i) K. Yoshida, Y. Shishikura, H. Takahashi, T. Imamoto, Org. Lett. 2008, 10, 2777-2780.
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(2008)
Org. Lett
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, pp. 2777-2780
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Yoshida, K.1
Shishikura, Y.2
Takahashi, H.3
Imamoto, T.4
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13
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0000585144
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Other reports on similar conversions: a D. Ma, X. Lu, Tetrahedron Lett. 1989, 30, 2109-2112;
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Other reports on similar conversions: a) D. Ma, X. Lu, Tetrahedron Lett. 1989, 30, 2109-2112;
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16
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0037414541
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d) T. Ishikawa, T. Mizuta, K. Hagiwara, T. Aikawa, T. Kudo, S. Saito, J. Org. Chem. 2003, 68, 3702-3705;
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(2003)
J. Org. Chem
, vol.68
, pp. 3702-3705
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Ishikawa, T.1
Mizuta, T.2
Hagiwara, K.3
Aikawa, T.4
Kudo, T.5
Saito, S.6
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18
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0037474669
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f) A. Coelho, E. Sotelo, E. Raviña, Tetrahedron 2003, 59, 2477-2484.
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(2003)
Tetrahedron
, vol.59
, pp. 2477-2484
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Coelho, A.1
Sotelo, E.2
Raviña, E.3
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20
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2942596792
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Angew. Chem. Int. Ed. 2004, 43, 2525-2527.
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(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 2525-2527
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21
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34250738498
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G. Gao, Q. Wang, X.-Y Yu, R.-G. Xie, L. Pu, Angew. Chem. 2006, 118, 128-131;
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(2006)
Angew. Chem
, vol.118
, pp. 128-131
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Gao, G.1
Wang, Q.2
Yu, X.-Y.3
Xie, R.-G.4
Pu, L.5
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22
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33745702289
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Angew. Chem. Int. Ed. 2006, 45, 122-125.
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(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 122-125
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23
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34447335324
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a) F. Yang, P. Xi, L. Yang, J. Lan, R. Xie, J. S. You, J. Org. Chem. 2007, 72, 5457-5460;
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(2007)
J. Org. Chem
, vol.72
, pp. 5457-5460
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Yang, F.1
Xi, P.2
Yang, L.3
Lan, J.4
Xie, R.5
You, J.S.6
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24
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30744477996
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another example of the asymmetric methyl propiolate addition to enals: B. M. Trost, A. H. Weiss, A. J. von Wangelin, J. Am. Chem. Soc. 2006, 128, 8-9.
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b) another example of the asymmetric methyl propiolate addition to enals: B. M. Trost, A. H. Weiss, A. J. von Wangelin, J. Am. Chem. Soc. 2006, 128, 8-9.
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25
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37049087368
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3 P was reported to remove the γ-oxygen of γ-hydroxy-α,β-acetylenic esters to give dienoates: C. Guo, X. Lu, J. Chem. Soc. Chem. Commun. 1993, 394-395;
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3 P was reported to remove the γ-oxygen of γ-hydroxy-α,β-acetylenic esters to give dienoates: C. Guo, X. Lu, J. Chem. Soc. Chem. Commun. 1993, 394-395;
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26
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73349127924
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3 P can also catalyze the conversion of α,β-acetylenic esters to dienoates: B. M. Trost, U. Kazmaier, J. Am. Chem. Soc. 1992, 114, 7933-7935.
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3 P can also catalyze the conversion of α,β-acetylenic esters to dienoates: B. M. Trost, U. Kazmaier, J. Am. Chem. Soc. 1992, 114, 7933-7935.
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