-
1
-
-
33846982970
-
-
I. Tellitu, S. Serna, M.T. Herrero, I. Moreno, E. Domínguez, and R. SanMartin J. Org. Chem. 72 2007 1526 1529
-
(2007)
J. Org. Chem.
, vol.72
, pp. 1526-1529
-
-
Tellitu, I.1
Serna, S.2
Herrero, M.T.3
Moreno, I.4
Domínguez, E.5
Sanmartin, R.6
-
2
-
-
22244442449
-
-
S. Serna, I. Tellitu, E. Domínguez, I. Moreno, and R. SanMartin Org. Lett. 7 2005 3073 3076
-
(2005)
Org. Lett.
, vol.7
, pp. 3073-3076
-
-
Serna, S.1
Tellitu, I.2
Domínguez, E.3
Moreno, I.4
Sanmartin, R.5
-
5
-
-
77954749600
-
-
L. Díaz, J. Bujons, J. Casas, A. Llebaria, and A. Delgado J. Med. Chem. 53 2010 5248 5255
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5248-5255
-
-
Díaz, L.1
Bujons, J.2
Casas, J.3
Llebaria, A.4
Delgado, A.5
-
7
-
-
11944256494
-
-
Some other biological activities have been also reported as chemotherapeutic agents against diabetes, cancer, and HIV. For some selected contributions on availability, synthesis and biological evaluation of polyhydroxylated indolizidines, see
-
M.L. Sinnott Chem. Rev. 90 1990 1171 1202 Some other biological activities have been also reported as chemotherapeutic agents against diabetes, cancer, and HIV. For some selected contributions on availability, synthesis and biological evaluation of polyhydroxylated indolizidines, see
-
(1990)
Chem. Rev.
, vol.90
, pp. 1171-1202
-
-
Sinnott, M.L.1
-
8
-
-
0030937840
-
-
F.M. Platt, G.R. Neises, G. Reinkensmeier, M.J. Townsend, V.H. Perry, R.L. Proia, B. Winchester, R.A. Dwek, and T.D. Butters Science 276 1997 428 431
-
(1997)
Science
, vol.276
, pp. 428-431
-
-
Platt, F.M.1
Neises, G.R.2
Reinkensmeier, G.3
Townsend, M.J.4
Perry, V.H.5
Proia, R.L.6
Winchester, B.7
Dwek, R.A.8
Butters, T.D.9
-
14
-
-
0028981092
-
-
R. Pili, J. Chang, R.A. Partis, R.A. Mueller, F.J. Chrest, and A. Passaniti Cancer Res. 55 1995 2920 2926
-
(1995)
Cancer Res.
, vol.55
, pp. 2920-2926
-
-
Pili, R.1
Chang, J.2
Partis, R.A.3
Mueller, R.A.4
Chrest, F.J.5
Passaniti, A.6
-
16
-
-
77952991718
-
-
X.-G. Hu, B. Bartholomew, R.J. Nash, F.X. Wilson, G.W.J. Fleet, S. Nakagawa, A. Kato, Y.-M. Jia, R. van Well, and C.-Y. Yu Org. Lett. 12 2010 2562 2565
-
(2010)
Org. Lett.
, vol.12
, pp. 2562-2565
-
-
Hu, X.-G.1
Bartholomew, B.2
Nash, R.J.3
Wilson, F.X.4
Fleet, G.W.J.5
Nakagawa, S.6
Kato, A.7
Jia, Y.-M.8
Van Well, R.9
Yu, C.-Y.10
-
17
-
-
46649095387
-
-
I. Izquierdo, J.A. Tamayo, M. Rodríguez, F. Franco, and D. Lo Re Tetrahedron 64 2008 7910 7913
-
(2008)
Tetrahedron
, vol.64
, pp. 7910-7913
-
-
Izquierdo, I.1
Tamayo, J.A.2
Rodríguez, M.3
Franco, F.4
Lo Re, D.5
-
19
-
-
77949818756
-
-
V. Zambrano, G. Rassu, A. Roggio, L. Pinna, F. Zanardi, C. Curti, G. Casiraghi, and L. Battistini Org. Biomol. Chem. 8 2010 1725 1730
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 1725-1730
-
-
Zambrano, V.1
Rassu, G.2
Roggio, A.3
Pinna, L.4
Zanardi, F.5
Curti, C.6
Casiraghi, G.7
Battistini, L.8
-
20
-
-
65949092546
-
-
Y.-S. Tian, J.-E. Joo, B.-S. Kong, V.-T. Pham, K.-Y. Lee, and W.-H. Ham J. Org. Chem. 74 2009 3962 3965
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3962-3965
-
-
Tian, Y.-S.1
Joo, J.-E.2
Kong, B.-S.3
Pham, V.-T.4
Lee, K.-Y.5
Ham, W.-H.6
-
23
-
-
41149161851
-
-
J.N. Abrams, R.S. Babu, H. Guo, D. Le, J. Le, J.M. Osbourn, and G.A. O'Doherty J. Org. Chem. 73 2008 1935 1940
-
(2008)
J. Org. Chem.
, vol.73
, pp. 1935-1940
-
-
Abrams, J.N.1
Babu, R.S.2
Guo, H.3
Le, D.4
Le, J.5
Osbourn, J.M.6
O'Doherty, G.A.7
-
29
-
-
33947727055
-
-
references therein
-
R. Chinchilla, and C. Nájera Chem. Rev. 107 2007 874 922 and references therein
-
(2007)
Chem. Rev.
, vol.107
, pp. 874-922
-
-
Chinchilla, R.1
Nájera, C.2
-
30
-
-
0000666195
-
-
(E)-β-bromostyrene was prepared as a single isomer from cinnamic acid by a modified catalytic Hunsdiecker reaction
-
(E)-β-bromostyrene was prepared as a single isomer from cinnamic acid by a modified catalytic Hunsdiecker reaction S. Chowdhury, and S. Roy J. Org. Chem. 62 1997 199 200
-
(1997)
J. Org. Chem.
, vol.62
, pp. 199-200
-
-
Chowdhury, S.1
Roy, S.2
-
34
-
-
64249149261
-
-
Y. Kiyotsuka, Y. Katayama, H.P. Acharya, T. Hyodo, and y. Kobayashi J. Org. Chem. 74 2009 1939 1951
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1939-1951
-
-
Kiyotsuka, Y.1
Katayama, Y.2
Acharya, H.P.3
Hyodo, T.4
Kobayashi, Y.5
-
36
-
-
0037122126
-
-
M. Arisawa, Y. Terada, M. Nakagawa, and A. Nishida Angew. Chem., Int. Ed. 41 2002 4732 4734
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4732-4734
-
-
Arisawa, M.1
Terada, Y.2
Nakagawa, M.3
Nishida, A.4
-
37
-
-
84859584116
-
-
See, for instance, the following selected reviews and the references cited therein
-
See, for instance, the following selected reviews and the references cited therein.
-
-
-
-
45
-
-
65549163116
-
-
This approach has been also applied in the synthesis of indolizidine skeleton. See
-
This approach has been also applied in the synthesis of indolizidine skeleton. See R. Ben-Othman, M. Othman, K. Ciamala, M. Knorr, C. Strohmann, and B. Decroix Tetrahedron 65 2009 4846 4854
-
(2009)
Tetrahedron
, vol.65
, pp. 4846-4854
-
-
Ben-Othman, R.1
Othman, M.2
Ciamala, K.3
Knorr, M.4
Strohmann, C.5
Decroix, B.6
-
46
-
-
33947255644
-
-
For a description of the combined use of several dihydroxylation methods, see: J.S. Reddy, and B.V. Rao J. Org. Chem. 72 2007 2224 2227
-
(2007)
J. Org. Chem.
, vol.72
, pp. 2224-2227
-
-
Reddy, J.S.1
Rao, B.V.2
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