-
3
-
-
0038222536
-
-
(a) Lebel, H.; Marcoux, J.-F.; Molinaro, C.; Charette, A. B. Chem. Rev. 2003, 103, 977.
-
(2003)
Chem. Rev
, vol.103
, pp. 977
-
-
Lebel, H.1
Marcoux, J.-F.2
Molinaro, C.3
Charette, A.B.4
-
7
-
-
36649025175
-
-
This type of reaction using 3-halo-1-alkenylsulfones was rarely studied, see: (a) Ogura, K, Iihama, T, Takahashi, K, Iida, H. Bull. Chem. Soc. Jpn. 1984, 57, 3347
-
This type of reaction using 3-halo-1-alkenylsulfones was rarely studied, see: (a) Ogura, K.; Iihama, T.; Takahashi, K.; Iida, H. Bull. Chem. Soc. Jpn. 1984, 57, 3347.
-
-
-
-
9
-
-
0034607673
-
-
(a) Ravindran, B.; Sakthivel, K.; Suresh, C. G.; Pathak, T. J. Org. Chem. 2000, 65, 2637.
-
(2000)
J. Org. Chem
, vol.65
, pp. 2637
-
-
Ravindran, B.1
Sakthivel, K.2
Suresh, C.G.3
Pathak, T.4
-
10
-
-
0037925372
-
-
(b) Sanki, A. K.; Suresh, C. G.; Falgune, U. D.; Pathak, T. Org. Lett. 2003, 5, 1285.
-
(2003)
Org. Lett
, vol.5
, pp. 1285
-
-
Sanki, A.K.1
Suresh, C.G.2
Falgune, U.D.3
Pathak, T.4
-
12
-
-
0013348708
-
-
(a) Baker, B. R.; Schaub, R. E.; Williams, J. H. J. Am. Chem. Soc. 1955, 77, 7.
-
(1955)
J. Am. Chem. Soc
, vol.77
, pp. 7
-
-
Baker, B.R.1
Schaub, R.E.2
Williams, J.H.3
-
13
-
-
0001753327
-
-
(b) Anderson, C. D.; Goodman, L.; Baker, B. R. J. Am. Chem. Soc. 1958, 80, 5247.
-
(1958)
J. Am. Chem. Soc
, vol.80
, pp. 5247
-
-
Anderson, C.D.1
Goodman, L.2
Baker, B.R.3
-
15
-
-
0042413539
-
-
(b) Montgomery, J. N.; Thorpe, M. C.; Clayton, S. D.; Thomas, H. J. Carbohydr. Res. 1974, 32, 404.
-
(1974)
Carbohydr. Res
, vol.32
, pp. 404
-
-
Montgomery, J.N.1
Thorpe, M.C.2
Clayton, S.D.3
Thomas, H.J.4
-
16
-
-
0040855707
-
-
(c) Bock, K.; Pedersen, C.; Thiem, J. Carbohydr. Res. 1979, 73, 85.
-
(1979)
Carbohydr. Res
, vol.73
, pp. 85
-
-
Bock, K.1
Pedersen, C.2
Thiem, J.3
-
17
-
-
0011406854
-
-
(d) Liptak, A.; Neszmelyi, A.; Kovac, P.; Hirsch, J. Tetrahedron 1981, 37, 2379.
-
(1981)
Tetrahedron
, vol.37
, pp. 2379
-
-
Liptak, A.1
Neszmelyi, A.2
Kovac, P.3
Hirsch, J.4
-
18
-
-
0019403969
-
-
(e) Su, T.-L.; Klein, R. S.; Fox, J. J. J. Org. Chem. 1981, 46, 1790.
-
(1981)
J. Org. Chem
, vol.46
, pp. 1790
-
-
Su, T.-L.1
Klein, R.S.2
Fox, J.J.3
-
19
-
-
0001084227
-
-
(f) Kawana, M.; Kuzuhara, H.; Emoto, S. Bull. Chem. Soc. Jpn. 1981, 54, 1492.
-
(1981)
Bull. Chem. Soc. Jpn
, vol.54
, pp. 1492
-
-
Kawana, M.1
Kuzuhara, H.2
Emoto, S.3
-
20
-
-
0000978425
-
-
(g) Kawana, M.; Koresawa, T.; Kuzuhara, H. Bull. Chem. Soc. Jpn. 1983, 56, 1095.
-
(1983)
Bull. Chem. Soc. Jpn
, vol.56
, pp. 1095
-
-
Kawana, M.1
Koresawa, T.2
Kuzuhara, H.3
-
21
-
-
0004498626
-
-
(a) Brimacombe, J. S.; Evans, M. E.; Forbes, E. J.; Foster, A. B.; Webber, J. M. Carbohydr. Res. 1967, 4, 239.
-
(1967)
Carbohydr. Res
, vol.4
, pp. 239
-
-
Brimacombe, J.S.1
Evans, M.E.2
Forbes, E.J.3
Foster, A.B.4
Webber, J.M.5
-
22
-
-
0015918096
-
-
(b) Sasaki, T.; Minamoto, K.; Suzuki, H. J. Org. Chem. 1973, 38, 598.
-
(1973)
J. Org. Chem
, vol.38
, pp. 598
-
-
Sasaki, T.1
Minamoto, K.2
Suzuki, H.3
-
24
-
-
23644457155
-
-
(d) Gagneron, J.; Gosselin, G.; Mathe, C. J. Org. Chem. 2005, 70, 6891.
-
(2005)
J. Org. Chem
, vol.70
, pp. 6891
-
-
Gagneron, J.1
Gosselin, G.2
Mathe, C.3
-
26
-
-
33748572631
-
-
(f) Besada, P.; Shin, D. H.; Costanzi, S.; Ko, H.; Mathe, C.; Gagneron, J.; Gosselin, G.; Maddileti, S.; Harden, T. K.; Jacobson, K. A. J. Med. Chem. 2006, 49, 5532.
-
(2006)
J. Med. Chem
, vol.49
, pp. 5532
-
-
Besada, P.1
Shin, D.H.2
Costanzi, S.3
Ko, H.4
Mathe, C.5
Gagneron, J.6
Gosselin, G.7
Maddileti, S.8
Harden, T.K.9
Jacobson, K.A.10
-
27
-
-
33846246048
-
-
(g) Nowak, I.; Cannon, J. F.; Robins, M. J. J. Org. Chem. 2007, 72, 532.
-
(2007)
J. Org. Chem
, vol.72
, pp. 532
-
-
Nowak, I.1
Cannon, J.F.2
Robins, M.J.3
-
28
-
-
36649014401
-
-
Schemes 8 and 9 represent a non-Michael addition approach to the synthesis of cyclopropanated carbohydrates containing an electron withdrawing group at C-3 of pentofuranosides, at is less efficient through Michael addition to vinyl sulfone-modified carbohydrates
-
Schemes 8 and 9 represent a non-Michael addition approach to the synthesis of cyclopropanated carbohydrates containing an electron withdrawing group at C-3 of pentofuranosides. This strategy may be explored when the introduction of a group at C-2 is less efficient through Michael addition to vinyl sulfone-modified carbohydrates.
-
This strategy may be explored when the introduction of a group
-
-
|