-
1
-
-
0033617178
-
-
For the synthesis and biological activities of α-methylene-γ-butyrolactams and α-alkylidene-γ-butyrolactams, see:
-
For the synthesis and biological activities of α-methylene-γ-butyrolactams and α-alkylidene-γ-butyrolactams, see:. Choudhury P.K., Foubelo F., and Yus M. J. Org. Chem. 64 (1999) 3376-3378
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3376-3378
-
-
Choudhury, P.K.1
Foubelo, F.2
Yus, M.3
-
4
-
-
18644380296
-
-
Janecki T., Blaszczyk E., Studzian K., Janecka A., Krajewska U., and Rozalski M. J. Med. Chem. 48 (2005) 3516-3521
-
(2005)
J. Med. Chem.
, vol.48
, pp. 3516-3521
-
-
Janecki, T.1
Blaszczyk, E.2
Studzian, K.3
Janecka, A.4
Krajewska, U.5
Rozalski, M.6
-
5
-
-
0032496946
-
-
Qiao L., Wang S., George C., Lewin N.E., Blumberg P.M., and Kozikowski A.P. J. Am. Chem. Soc. 120 (1998) 6629-6630
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 6629-6630
-
-
Qiao, L.1
Wang, S.2
George, C.3
Lewin, N.E.4
Blumberg, P.M.5
Kozikowski, A.P.6
-
12
-
-
0000677635
-
-
For the ring-opening reactions of aziridine derivatives, see:
-
For the ring-opening reactions of aziridine derivatives, see:. Sabitha G., Babu S., Rajkumar M., and Yadav J.S. Org. Lett. 4 (2002) 343-345
-
(2002)
Org. Lett.
, vol.4
, pp. 343-345
-
-
Sabitha, G.1
Babu, S.2
Rajkumar, M.3
Yadav, J.S.4
-
24
-
-
0001330004
-
-
For the synthesis and stereochemistry of aziridines involving sulfur ylide chemistry, see:
-
For the synthesis and stereochemistry of aziridines involving sulfur ylide chemistry, see:. Li A.-H., Dai L.-X., Hou X.-L., and Chen M.-B. J. Org. Chem. 61 (1996) 4641-4648
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4641-4648
-
-
Li, A.-H.1
Dai, L.-X.2
Hou, X.-L.3
Chen, M.-B.4
-
29
-
-
33846938853
-
-
note
-
3S: C, 68.11; H, 4.76; N, 5.30. Found: C, 68.23; H, 4.92; N, 5.19.
-
-
-
-
30
-
-
0001328716
-
-
For the synthesis and biological activities of α-methylene-γ-butyrolactones and α-alkylidene-γ-butyrolactones, see:
-
For the synthesis and biological activities of α-methylene-γ-butyrolactones and α-alkylidene-γ-butyrolactones, see:. Bauchat P., Le Rouille E., and Foucaud A. Bull. Soc. Chim. Fr. 128 (1991) 267-271
-
(1991)
Bull. Soc. Chim. Fr.
, vol.128
, pp. 267-271
-
-
Bauchat, P.1
Le Rouille, E.2
Foucaud, A.3
-
36
-
-
0043172234
-
-
Pohmakotr M., Sampaongoen L., Issaree A., Tuchinda P., and Reutrakul V. Tetrahedron Lett. 44 (2003) 6717-6720
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6717-6720
-
-
Pohmakotr, M.1
Sampaongoen, L.2
Issaree, A.3
Tuchinda, P.4
Reutrakul, V.5
-
40
-
-
0030023919
-
-
Lee J., Sharma R., Wang S., Milne G.W.A., Lewin N.E., Szallasi Z., Blumberg P.M., George C., and Marquez V.E. J. Med. Chem. 39 (1996) 36-45
-
(1996)
J. Med. Chem.
, vol.39
, pp. 36-45
-
-
Lee, J.1
Sharma, R.2
Wang, S.3
Milne, G.W.A.4
Lewin, N.E.5
Szallasi, Z.6
Blumberg, P.M.7
George, C.8
Marquez, V.E.9
-
42
-
-
34249098881
-
-
For the examples of cyclization involving the ester moiety, see:
-
For the examples of cyclization involving the ester moiety, see:. Alvernhe G., Lacombe S., Laurent A., and Marquet B. J. Chem. Res. (1980) 54-55
-
(1980)
J. Chem. Res.
, pp. 54-55
-
-
Alvernhe, G.1
Lacombe, S.2
Laurent, A.3
Marquet, B.4
-
46
-
-
33846903904
-
-
note
-
4S: C, 59.02; H, 3.92; N, 2.87. Found: C, 58.91; H, 3.89; N, 2.94.
-
-
-
|