-
2
-
-
0000785058
-
-
b) A. Fürstner, Angew. Chem. 2000, 112, 3140; Angew. Chem. Int. Ed. 2000, 39, 3012;
-
(2000)
Angew. Chem.
, vol.112
, pp. 3140
-
-
Fürstner, A.1
-
3
-
-
0001399412
-
-
b) A. Fürstner, Angew. Chem. 2000, 112, 3140; Angew. Chem. Int. Ed. 2000, 39, 3012;
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3012
-
-
-
9
-
-
0000063152
-
-
h) M. Schuster, S. Blechert, Angew. Chem. 1997, 109, 2124; Angew. Chem. Int. Ed. Engl. 1997, 36, 2036.
-
(1997)
Angew. Chem.
, vol.109
, pp. 2124
-
-
Schuster, M.1
Blechert, S.2
-
10
-
-
0030771019
-
-
h) M. Schuster, S. Blechert, Angew. Chem. 1997, 109, 2124; Angew. Chem. Int. Ed. Engl. 1997, 36, 2036.
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 2036
-
-
-
11
-
-
0037205933
-
-
For recent theoretical studies of the mechanism of the ruthenium-catalyzed olefin metathesis, see: i) L. Cavallo, J. Am. Chem. Soc. 2002, 124, 8965;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 8965
-
-
Cavallo, L.1
-
12
-
-
0037009091
-
-
j) S. F. Vyboishchikov, M. Bühl, W. Thiel, Chem. Eur. J. 2002, 8, 3962;
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 3962
-
-
Vyboishchikov, S.F.1
Bühl, M.2
Thiel, W.3
-
13
-
-
0347449829
-
-
k) C. Adlhart, P. Chen, Angew. Chem. 2002, 114, 4668; Angew. Chem. Int. Ed. 2002, 41, 4484.
-
(2002)
Angew. Chem.
, vol.114
, pp. 4668
-
-
Adlhart, C.1
Chen, P.2
-
14
-
-
0037011321
-
-
k) C. Adlhart, P. Chen, Angew. Chem. 2002, 114, 4668; Angew. Chem. Int. Ed. 2002, 41, 4484.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 4484
-
-
-
15
-
-
0033593413
-
-
For the unexpected reactivity of the Grubbs catalyst for Kharasch addition, see: J. A. Tallarico, L. A. Malnick, M. L. Snapper, J. Org. Chem. 1999, 64, 344.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 344
-
-
Tallarico, J.A.1
Malnick, L.A.2
Snapper, M.L.3
-
16
-
-
0037009701
-
-
For the Grubbs carbene promoted activation of silanes in the presence of carbonyls, see: S. V. Maifeld, R. L. Miller, D. Lee, Tetrahedron Lett. 2002, 43, 6363.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6363
-
-
Maifeld, S.V.1
Miller, R.L.2
Lee, D.3
-
18
-
-
33751154638
-
-
b) H. Doucet, B. Martín-Vaca, C. Bruneau, P. H. Dixneuf, J. Org. Chem. 1995, 60, 7247.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 7247
-
-
Doucet, H.1
Martín-Vaca, B.2
Bruneau, C.3
Dixneuf, P.H.4
-
19
-
-
0001855961
-
-
a) P. Schwab, R. H. Grubbs, J. W. Ziller, J. Am. Chem. Soc. 1996, 118, 100.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 100
-
-
Schwab, P.1
Grubbs, R.H.2
Ziller, J.W.3
-
20
-
-
0037451439
-
-
For a review on nonmetathetic behavior patterns of the Grubbs carbene, see: b) B. Alcaide, P. Almendros, Chem. Eur. J. 2003, 9, 1258.
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 1258
-
-
Alcaide, B.1
Almendros, P.2
-
21
-
-
0003463148
-
-
Wiley, New York
-
a) T. W. Greene, G. M. Wuts, Protective Groups in Organic Synthesis, 3rd ed., Wiley, New York, 1999;
-
(1999)
Protective Groups in Organic Synthesis, 3rd Ed.
-
-
Greene, T.W.1
Wuts, G.M.2
-
24
-
-
0001115594
-
-
d) M. Schelhaas, H. Waldmann, Angew. Chem. 1996, 108, 2192; Angew. Chem. Int. Ed. Engl. 1996, 35, 2056.
-
(1996)
Angew. Chem.
, vol.108
, pp. 2192
-
-
Schelhaas, M.1
Waldmann, H.2
-
25
-
-
0029799743
-
-
d) M. Schelhaas, H. Waldmann, Angew. Chem. 1996, 108, 2192; Angew. Chem. Int. Ed. Engl. 1996, 35, 2056.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 2056
-
-
-
26
-
-
0032568384
-
-
For a review, see: F. Guibé, Tetrahedron 1998, 54, 2967.
-
(1998)
Tetrahedron
, vol.54
, pp. 2967
-
-
Guibé, F.1
-
27
-
-
0001272378
-
-
For a preliminary communication of a part of this work, see: B. Alcaide, P. Almendros, J. M. Alonso, M. F. Aly, Org. Lett. 2001, 3, 3781.
-
(2001)
Org. Lett.
, vol.3
, pp. 3781
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Aly, M.F.4
-
28
-
-
0017383282
-
-
A cleavage of allyl amines which needs 100% rhodium catalyst was reported some years ago: a) B. Moreau, S. Lavielle, A. Marquet, Tetrahedron Lett. 1977, 18, 2591.
-
(1977)
Tetrahedron Lett.
, vol.18
, pp. 2591
-
-
Moreau, B.1
Lavielle, S.2
Marquet, A.3
-
31
-
-
0036971398
-
-
II complexes, see: b) M. E. Morilla, G. Morfes, M. C. Nicasio, T. R. Belderrain, M. M. Díaz-Requejo, C. Graiff, A. Tiripicchio, R. Sánchez-Delgado, P. J. Pérez, Chem. Commun. 2002, 1848.
-
(2002)
Chem. Commun.
, vol.1848
-
-
Morilla, M.E.1
Morfes, G.2
Nicasio, M.C.3
Belderrain, T.R.4
Díaz-Requejo, M.M.5
Graiff, C.6
Tiripicchio, A.7
Sánchez-Delgado, R.8
Pérez, P.J.9
-
32
-
-
0037006835
-
-
See, for instance: a) B. Alcaide, P. Almendros, C. Aragoncillo, Chem. Eur. J. 2002, 8, 1719;
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 1719
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
33
-
-
0036305317
-
-
b) B. Alcaide, P. Almendros, C. Aragoncillo, M. C. Redondo, Chem. Commun. 2002, 1472;
-
(2002)
Chem. Commun.
, pp. 1472
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
Redondo, M.C.4
-
35
-
-
0037155509
-
-
d) B. Alcaide, P. Almendros, R. Rodríguez-Acebes, J. Org. Chem. 2002, 67, 1925;
-
(2002)
J. Org. Chem.
, vol.67
, pp. 1925
-
-
Alcaide, B.1
Almendros, P.2
Rodríguez-Acebes, R.3
-
36
-
-
0037019993
-
-
e) B. Alcaide, P. Almendros, J. M. Alonso, M. F. Aly, C. Pardo, E. Sáez, M. R. Torres, J. Org. Chem. 2002, 67, 7004;
-
(2002)
J. Org. Chem.
, vol.67
, pp. 7004
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Aly, M.F.4
Pardo, C.5
Sáez, E.6
Torres, M.R.7
-
37
-
-
0242670017
-
-
f) B. Alcaide, P. Almendros, J. M. Alonso, M. C. Redondo, J. Org. Chem. 2003, 68, 1426.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 1426
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Redondo, M.C.4
-
38
-
-
0035479564
-
-
For the ruthenium-promoted isomerization of N-allyl amides to enamides, see: a) S. Krompiec, M. Pigulla, W. Szczepankiewicz, T. Bieg, N. Kuznik, K. Leszczynska-Sejda, M. Kubicki, T. Borowiak, Tetrahedron Lett. 2002, 42, 7095;
-
(2002)
Tetrahedron Lett.
, vol.42
, pp. 7095
-
-
Krompiec, S.1
Pigulla, M.2
Szczepankiewicz, W.3
Bieg, T.4
Kuznik, N.5
Leszczynska-Sejda, K.6
Kubicki, M.7
Borowiak, T.8
-
39
-
-
0000535557
-
-
b) S. S. Kinderman, J.-H. van Maarseveen, H. E. Schoemaker, H. Hiemstra, F. P. J. T. Rutjes, Org. Lett. 2001, 3, 2045;
-
(2001)
Org. Lett.
, vol.3
, pp. 2045
-
-
Kinderman, S.S.1
Van Maarseveen, J.-H.2
Schoemaker, H.E.3
Hiemstra, H.4
Rutjes, F.P.J.T.5
-
43
-
-
0037073212
-
-
For several reports noting related ruthenium-catalyzed isomerizations, see ref. [5b]. Since our preliminary communication, it has been reported that the second-generation Grubbs carbene is able to mediate isomerization of allyl ethers to the corresponding vinyl ethers: a) A. E. Sutton, B. A. Seigal, D. F. Finnegan, M. L. Snapper, J. Am. Chem. Soc. 2002, 124, 13 390;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 13390
-
-
Sutton, A.E.1
Seigal, B.A.2
Finnegan, D.F.3
Snapper, M.L.4
-
44
-
-
0037017679
-
-
b) C. Cadot, P. I. Dalko, J. Cossy, Tetrahedron Lett. 2002, 43, 1839;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 1839
-
-
Cadot, C.1
Dalko, P.I.2
Cossy, J.3
-
46
-
-
0142014454
-
-
There has also been a report that an isomerization of a terminal olefin to the internal alkene by using the second-generation Grubbs carbene proceeds faster than RCM: d) M. Arisawa, Y. Terada, M. Nakagawa, A. Nishida, Angew. Chem. 2002, 114, 4926; Angew. Chem. Int. Ed. 2002, 41, 4732.
-
(2002)
Angew. Chem.
, vol.114
, pp. 4926
-
-
Arisawa, M.1
Terada, Y.2
Nakagawa, M.3
Nishida, A.4
-
47
-
-
0037122126
-
-
There has also been a report that an isomerization of a terminal olefin to the internal alkene by using the second-generation Grubbs carbene proceeds faster than RCM: d) M. Arisawa, Y. Terada, M. Nakagawa, A. Nishida, Angew. Chem. 2002, 114, 4926; Angew. Chem. Int. Ed. 2002, 41, 4732.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 4732
-
-
-
48
-
-
0037420362
-
-
a) T. M. Trnka, J. P. Morgan, M. S. Sanford, T. E. Wilhelm, M. Scholl, T.-L. Choi, S. Ding, M. W. Day, R. H. Grubbs, J. Am. Chem. Soc. 2003, 125, 2546;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2546
-
-
Trnka, T.M.1
Morgan, J.P.2
Sanford, M.S.3
Wilhelm, T.E.4
Scholl, M.5
Choi, T.-L.6
Ding, S.7
Day, M.W.8
Grubbs, R.H.9
-
50
-
-
0037833492
-
-
c) B. Cetinkaya, S. Demir, I. Özdemir, L. Toupet, D. Sémeril, C. Bruneau, P. H. Dixneuf, Chem. Eur. J. 2003, 9, 2323;
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 2323
-
-
Cetinkaya, B.1
Demir, S.2
Özdemir, I.3
Toupet, L.4
Sémeril, D.5
Bruneau, C.6
Dixneuf, P.H.7
-
51
-
-
0037463719
-
-
d) A. M. Dunne, S. Mix, S. Blechert, Tetrahedron Lett. 2003, 44, 2733;
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 2733
-
-
Dunne, A.M.1
Mix, S.2
Blechert, S.3
-
52
-
-
0037050473
-
-
e) J. P. Morgan, C. Morrill, R. H. Grubbs, Org. Lett. 2002, 4, 67;
-
(2002)
Org. Lett.
, vol.4
, pp. 67
-
-
Morgan, J.P.1
Morrill, C.2
Grubbs, R.H.3
-
53
-
-
0001174034
-
-
f) H. Wakamatsu, S. Blechert, Angew. Chem. 2002, 114, 2509; Angew. Chem. Int. Ed. 2002, 41, 2403;
-
(2002)
Angew. Chem.
, vol.114
, pp. 2509
-
-
Wakamatsu, H.1
Blechert, S.2
-
54
-
-
0037007937
-
-
f) H. Wakamatsu, S. Blechert, Angew. Chem. 2002, 114, 2509; Angew. Chem. Int. Ed. 2002, 41, 2403;
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2403
-
-
-
55
-
-
0035914638
-
-
g) A. Fürstner, O. Guth, A. Düffels, G. Seidel, M. Liebl, B. Gabor, R. Mynott, Chem. Eur. J. 2001, 7, 4811;
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 4811
-
-
Fürstner, A.1
Guth, O.2
Düffels, A.3
Seidel, G.4
Liebl, M.5
Gabor, B.6
Mynott, R.7
-
56
-
-
0035800494
-
-
h) A. Fürstner, L. Ackermann, B. Gabor, R. Goddard, C. W. Lehmann, R. Mynott, F. Stelzer, O. R. Thiel, Chem. Eur. J. 2001, 7, 3236;
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 3236
-
-
Fürstner, A.1
Ackermann, L.2
Gabor, B.3
Goddard, R.4
Lehmann, C.W.5
Mynott, R.6
Stelzer, F.7
Thiel, O.R.8
-
58
-
-
0034734340
-
-
j) S. B. Garber, J. S. Kingsbury, B. L. Gray, A. H. Hoveyda, J. Am. Chem. Soc. 2000, 122, 8168;
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 8168
-
-
Garber, S.B.1
Kingsbury, J.S.2
Gray, B.L.3
Hoveyda, A.H.4
-
59
-
-
0037620216
-
-
k) A. Fürstner, O. R. Thiel, L. Ackermann, H.-J. Schanz, S. Nolan, J. Org. Chem. 2000, 65, 2204.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 2204
-
-
Fürstner, A.1
Thiel, O.R.2
Ackermann, L.3
Schanz, H.-J.4
Nolan, S.5
-
60
-
-
78249281266
-
-
G. C. Fu, S. T. Nguyen, R. H. Grubbs, J. Am. Chem. Soc. 1993, 115, 9856.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9856
-
-
Fu, G.C.1
Nguyen, S.T.2
Grubbs, R.H.3
-
61
-
-
77956830705
-
-
(Ed.: G. A. Cordell), Academic Press, San Diego, Chapter 4
-
The isomeric pyrrolidino[2,1-a]isoquinoline nucleus represents a structural fragment of the erytrinan alkaloids, which possess antidepressant, muscarinic agonist, and antileukemic properties. For a review on erythrinanes, see: a) Y. Tsuda, T. Sano in The Alkaloids: Chemistry and Pharmacology, Vol. 48 (Ed.: G. A. Cordell), Academic Press, San Diego, 1996, Chapter 4, pp. 249.
-
(1996)
The Alkaloids: Chemistry and Pharmacology
, vol.48
, pp. 249
-
-
Tsuda, Y.1
Sano, T.2
-
63
-
-
0037185570
-
-
For selected examples, see: a) X. Ginesta, M. A. Pericás, A. Riera, Tetrahedron Lett. 2002, 43, 779;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 779
-
-
Ginesta, X.1
Pericás, M.A.2
Riera, A.3
-
64
-
-
0036134489
-
-
b) N. U. Sata, R. Kuwahara, Y. Murata, Tetrahedron Lett. 2002, 43, 115.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 115
-
-
Sata, N.U.1
Kuwahara, R.2
Murata, Y.3
-
65
-
-
0034758814
-
-
Their interesting biological activities include antiviral, antitumor, and glucosidase inhibition activities. For selected reviews, see: a) J. P. Michael, Nat. Prod. Rep. 2001, 18, 520;
-
(2001)
Nat. Prod. Rep.
, vol.18
, pp. 520
-
-
Michael, J.P.1
-
66
-
-
0031976212
-
-
b) A. J. Vlietinck, T. De Bruyne, S. Apers, L. A. Pieters, Planta Med. 1998, 64, 97;
-
(1998)
Planta Med.
, vol.64
, pp. 97
-
-
Vlietinck, A.J.1
De Bruyne, T.2
Apers, S.3
Pieters, L.A.4
-
70
-
-
0000168392
-
-
f) M. Ikeda, T. Sato, H. Ishibashi, Heterocycles 1988, 27, 1465.
-
(1988)
Heterocycles
, vol.27
, pp. 1465
-
-
Ikeda, M.1
Sato, T.2
Ishibashi, H.3
-
71
-
-
0041345738
-
-
a) B. Alcaide, P. Almendros, J. M. Alonso, M. F. Aly, Chem. Eur. J. 2003, 9, 3415-3426;
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 3415-3426
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Aly, M.F.4
-
72
-
-
0034805899
-
-
b) B. Alcaide, P. Almendros, J. M. Alonso, M. F. Aly, M. R. Torres, Synlett 2001, 1531.
-
(2001)
Synlett
, pp. 1531
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
Aly, M.F.4
Torres, M.R.5
-
74
-
-
0347449830
-
-
note
-
Full spectroscopic and analytical data for compounds not included in this Experimental Section are described in the Supporting Information.
-
-
-
|