-
1
-
-
27544497732
-
-
Tsuji J. (Ed), Springer, Berlin/Heidelberg
-
In: Tsuji J. (Ed). Palladium in Organic Synthesis (2005), Springer, Berlin/Heidelberg
-
(2005)
Palladium in Organic Synthesis
-
-
-
2
-
-
0030878188
-
-
and cited refs
-
Nicolaou K.C., Shi G.Q., Gunzner J.L., Gärtner P., and Yang Z. J. Am. Chem. Soc. 119 (1997) 5467 and cited refs
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5467
-
-
Nicolaou, K.C.1
Shi, G.Q.2
Gunzner, J.L.3
Gärtner, P.4
Yang, Z.5
-
12
-
-
0033608115
-
-
Jiang J., DeVita R.J., Doss G.A., Goulet M.T., and Wyvratt M.J. J. Am. Chem. Soc. 121 (1999) 593
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 593
-
-
Jiang, J.1
DeVita, R.J.2
Doss, G.A.3
Goulet, M.T.4
Wyvratt, M.J.5
-
13
-
-
0343820082
-
-
Coudert G., Buon C., Chacun-Lefevre L., Rabot R., and Bouyssou P. Tetrahedron 56 (2000) 605
-
(2000)
Tetrahedron
, vol.56
, pp. 605
-
-
Coudert, G.1
Buon, C.2
Chacun-Lefevre, L.3
Rabot, R.4
Bouyssou, P.5
-
15
-
-
34547615213
-
-
Cottineau B., Gillaizeau I., Farard J., Auclair M., and Coudert G. Synlett 12 (2007) 1925
-
(2007)
Synlett
, vol.12
, pp. 1925
-
-
Cottineau, B.1
Gillaizeau, I.2
Farard, J.3
Auclair, M.4
Coudert, G.5
-
20
-
-
0035817206
-
-
The following works dealt with the stability problem in cyclic ketene aminal phosphates and triflates. Our experience has shown that the acyclic counterparts may be as labile as the ones derived from five-membered lactams (Ref. 8a):
-
The following works dealt with the stability problem in cyclic ketene aminal phosphates and triflates. Our experience has shown that the acyclic counterparts may be as labile as the ones derived from five-membered lactams (Ref. 8a):. Lepifre F., Clavier S., Bouyssou P., and Coudert G. Tetrahedron 57 (2001) 6969
-
(2001)
Tetrahedron
, vol.57
, pp. 6969
-
-
Lepifre, F.1
Clavier, S.2
Bouyssou, P.3
Coudert, G.4
-
21
-
-
70350755145
-
-
See Ref. 3c
-
See Ref. 3c.
-
-
-
-
31
-
-
57349154042
-
-
Simas A.B.C., de Sales D.L., Cavalcante S.F.A., de Medeiros C.M., Moraes S.H.S., and de Carvalho E.M. Lett. Org. Chem. 5 (2008) 587
-
(2008)
Lett. Org. Chem.
, vol.5
, pp. 587
-
-
Simas, A.B.C.1
de Sales, D.L.2
Cavalcante, S.F.A.3
de Medeiros, C.M.4
Moraes, S.H.S.5
de Carvalho, E.M.6
-
32
-
-
51049124099
-
-
Stannane 17b was prepared by hydrostannylation of 3-butyn-1-ol under the conditions advanced by Chong's group, followed by O-methylation:
-
Stannane 17b was prepared by hydrostannylation of 3-butyn-1-ol under the conditions advanced by Chong's group, followed by O-methylation:. Darwish A., Lang A., Kim T., and Chong J.M. Org. Lett. 10 (2008) 861
-
(2008)
Org. Lett.
, vol.10
, pp. 861
-
-
Darwish, A.1
Lang, A.2
Kim, T.3
Chong, J.M.4
-
35
-
-
70350776023
-
-
note
-
+).
-
-
-
-
36
-
-
70350781897
-
-
note
-
-1.
-
-
-
-
37
-
-
0030593682
-
-
Enynes and dienes displaying similar functional features, for the most part, have been incidentally generated:
-
Enynes and dienes displaying similar functional features, for the most part, have been incidentally generated:. Meffre P., Gauzy L., Branquet E., Durand P., and Le Goffic F. Tetrahedron 52 (1996) 11215
-
(1996)
Tetrahedron
, vol.52
, pp. 11215
-
-
Meffre, P.1
Gauzy, L.2
Branquet, E.3
Durand, P.4
Le Goffic, F.5
-
39
-
-
0034647926
-
-
For a designed methodology towards similar enyne via a double elimination:
-
For a designed methodology towards similar enyne via a double elimination:. Saito S., Uchiyama N., Gevorgyan V., and Yamamoto Y. J. Org. Chem. 65 (2001) 4338
-
(2001)
J. Org. Chem.
, vol.65
, pp. 4338
-
-
Saito, S.1
Uchiyama, N.2
Gevorgyan, V.3
Yamamoto, Y.4
|