-
2
-
-
0002149739
-
-
A. P. Schaap, L. Lopez, S. D. Anderson, S. D. Gagnon, Tetrahedron Lett. 1982, 23, 5493-5496.
-
(1982)
Tetrahedron Lett
, vol.23
, pp. 5493-5496
-
-
Schaap, A.P.1
Lopez, L.2
Anderson, S.D.3
Gagnon, S.D.4
-
3
-
-
0034922306
-
-
Recent examples: a O. G. Kulinkovich, D. A. Astashko, V. I. Tyvorskii, N. A. Ilyina, Synthesis 2001, 1453-1455;
-
Recent examples: a) O. G. Kulinkovich, D. A. Astashko, V. I. Tyvorskii, N. A. Ilyina, Synthesis 2001, 1453-1455;
-
-
-
-
4
-
-
0041807557
-
-
b) T. Tokuyasu, S. Kunikawa, A. Masuyama, M. Nojima, Org. Lett. 2002, 4, 3595-3598;
-
(2002)
Org. Lett
, vol.4
, pp. 3595-3598
-
-
Tokuyasu, T.1
Kunikawa, S.2
Masuyama, A.3
Nojima, M.4
-
5
-
-
0042868645
-
-
c) H. Ikeda, K. Akiyama, Y. Takahashi, T. Nakamura, S. Ishizaki, Y. Shiratori, H. Ohaku, J. L. Goodman, A. Houmam, D. D. M. Wayner, S. Tero-Kubota, T. Miyashi, J. Am. Chem. Soc. 2003, 125, 9147-9157;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 9147-9157
-
-
Ikeda, H.1
Akiyama, K.2
Takahashi, Y.3
Nakamura, T.4
Ishizaki, S.5
Shiratori, Y.6
Ohaku, H.7
Goodman, J.L.8
Houmam, A.9
Wayner, D.D.M.10
Tero-Kubota, S.11
Miyashi, T.12
-
6
-
-
17644416367
-
-
d) H. Shimizu, S. Onitsuka, H. Egami, T. Katsuki, J. Am. Chem. Soc. 2005, 127, 5396-5413;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 5396-5413
-
-
Shimizu, H.1
Onitsuka, S.2
Egami, H.3
Katsuki, T.4
-
7
-
-
17844383740
-
-
e) M. Kirihara, H. Kakuda, M. Ichinose, Y. Ochiai, S. Takizawa, A. Mokuya, K. Okubo, A. Hatano, M. Shiro, Tetrahedron 2005, 61, 4831-4839.
-
(2005)
Tetrahedron
, vol.61
, pp. 4831-4839
-
-
Kirihara, M.1
Kakuda, H.2
Ichinose, M.3
Ochiai, Y.4
Takizawa, S.5
Mokuya, A.6
Okubo, K.7
Hatano, A.8
Shiro, M.9
-
11
-
-
0035861032
-
-
To the best of our knowledge, there is only one report in the literature showing cyclic voltammetry performed on cyclopropylamines: H. B. Lee, M. J. Sung, S. C. Blackstock, J. K. Cha, J. Am. Chem. Soc. 2001, 123, 11322-11324; see also Supporting Information.
-
To the best of our knowledge, there is only one report in the literature showing cyclic voltammetry performed on cyclopropylamines: H. B. Lee, M. J. Sung, S. C. Blackstock, J. K. Cha, J. Am. Chem. Soc. 2001, 123, 11322-11324; see also Supporting Information.
-
-
-
-
15
-
-
0001891487
-
-
Ed, I. Marek, Wiley-VCH, Weinheim
-
c) A. de Meijere, S. I. Kozhushkov, A. I. Savchenko in Titanium and Zirconium in Organic Synthesis (Ed.: I. Marek), Wiley-VCH, Weinheim, 2002, pp. 390-434;
-
(2002)
Titanium and Zirconium in Organic Synthesis
, pp. 390-434
-
-
de Meijere, A.1
Kozhushkov, S.I.2
Savchenko, A.I.3
-
16
-
-
2542493171
-
-
d) A. de Meijere, S. I. Kozhushkov, A. I. Savchenko, J. Organomet. Chem. 2004, 689, 2033-2055.
-
(2004)
J. Organomet. Chem
, vol.689
, pp. 2033-2055
-
-
de Meijere, A.1
Kozhushkov, S.I.2
Savchenko, A.I.3
-
19
-
-
35649002494
-
-
The stable endoperoxides previously synthesized in our laboratory also featured this extra subsitution on the dioxolane system. See Ref, 5
-
The stable endoperoxides previously synthesized in our laboratory also featured this extra subsitution on the dioxolane system. See Ref. [5].
-
-
-
-
20
-
-
0346705252
-
-
For a review covering new antimalarial drugs, see
-
For a review covering new antimalarial drugs, see: J. Wiesner, R. Ortmann, H. Jomaa, M. Schlitzer, Angew. Chem. 2003, 115, 5432-5451;
-
(2003)
Angew. Chem
, vol.115
, pp. 5432-5451
-
-
Wiesner, J.1
Ortmann, R.2
Jomaa, H.3
Schlitzer, M.4
-
21
-
-
0344875966
-
-
Angew. Chem. Int. Ed. 2003, 42, 5274-5293.
-
(2003)
Chem. Int. Ed
, vol.42
, pp. 5274-5293
-
-
Angew1
-
22
-
-
23744478677
-
-
and references therein. 2005
-
A. Robert, F. Benoit-Vical, B. Meunier, Coord. Chem. Rev. 2005, 249, 1927-1936, and references therein.
-
(1927)
Coord. Chem. Rev
, vol.249
-
-
Robert, A.1
Benoit-Vical, F.2
Meunier, B.3
-
23
-
-
35648936413
-
-
90 = 0.21 μM.
-
90 = 0.21 μM.
-
-
-
-
24
-
-
35648947827
-
-
The cis and trans diastereoisomers are defined according to the relative configurations of the amine and the 2-( tert-butyldimethylsilyloxy)ethyl substituents of the dioxolane ring.
-
The cis and trans diastereoisomers are defined according to the relative configurations of the amine and the 2-( tert-butyldimethylsilyloxy)ethyl substituents of the dioxolane ring.
-
-
-
|