-
1
-
-
0030058793
-
-
For a review on strategies in oligosaccharides synthesis, see: Boons, G.-J. Tetrahedron 1996, 52, 1095.
-
(1996)
Tetrahedron
, vol.52
, pp. 1095
-
-
Boons, G.-J.1
-
3
-
-
0027772575
-
-
(a) Boons, G.-J.; Grice, P.; Leslie, R.; Ley, S. V.; Yeung, L. L. Tetrahedron Lett. 1993, 34, 8523.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 8523
-
-
Boons, G.-J.1
Grice, P.2
Leslie, R.3
Ley, S.V.4
Yeung, L.L.5
-
4
-
-
33748652692
-
-
(b) Grice, P.; Ley, S. V.; Pietruszka, J.; Priepke, H. W. M.; Warriner, S. L. J. Chem. Soc., Perkin Trans, 1 1997, 351.
-
(1997)
J. Chem. Soc., Perkin Trans, 1
, pp. 351
-
-
Grice, P.1
Ley, S.V.2
Pietruszka, J.3
Priepke, H.W.M.4
Warriner, S.L.5
-
5
-
-
33748601612
-
-
(c) Douglas, N. L.; Ley, S. V.; Lucking, U.; Warriner, S. L. J. Chem. Soc., Perkin Trans, 1 1998, 51.
-
(1998)
J. Chem. Soc., Perkin Trans, 1
, pp. 51
-
-
Douglas, N.L.1
Ley, S.V.2
Lucking, U.3
Warriner, S.L.4
-
6
-
-
0033518559
-
-
Zhang, Z.; Ollmann, I. R.; Ye, X.; Wischnat, R.; Baasov, T.; Wong, C.-H. J. Am. Chem. Soc. 1999, 121, 734.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 734
-
-
Zhang, Z.1
Ollmann, I.R.2
Ye, X.3
Wischnat, R.4
Baasov, T.5
Wong, C.-H.6
-
7
-
-
85022498621
-
-
Fraser-Reid, B.; Udodong, U. E.; Wu, Z.; Ottosson, H.; Merritt, J. R.; Rao, C. S.; Roberts, C.; Madsen, R. Synlett 1992, 927.
-
(1992)
Synlett
, pp. 927
-
-
Fraser-Reid, B.1
Udodong, U.E.2
Wu, Z.3
Ottosson, H.4
Merritt, J.R.5
Rao, C.S.6
Roberts, C.7
Madsen, R.8
-
10
-
-
0030830477
-
-
Hashimoto, S.; Sakamoto, H.; Honda, T.; Abe, H.; Nakamura, S.; Ikegami, S. Tetrahedron Lett. 1997, 38, 8969.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8969
-
-
Hashimoto, S.1
Sakamoto, H.2
Honda, T.3
Abe, H.4
Nakamura, S.5
Ikegami, S.6
-
11
-
-
0029116046
-
-
(a) Boons, G.-J.; Geurtsen, R.; Holmes, D. Tetrahedron Lett. 1995, 36, 6325.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 6325
-
-
Boons, G.-J.1
Geurtsen, R.2
Holmes, D.3
-
12
-
-
0000469759
-
-
(b) Geurtsen, R.; Holmes, D. S.; Boons, G.-J. J. Org. Chem. 1997, 62, 8145.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 8145
-
-
Geurtsen, R.1
Holmes, D.S.2
Boons, G.-J.3
-
13
-
-
0035955202
-
-
During the preparation of this manuscript, Kerns et al. reported the use of oxazolidinone protected glucosamine derivatives for the synthesis of α-linked 2-amino glycosides. Benakli, K.; Zha, C.; Kerns, R. J. J. Am. Chem. Soc. 2001, 123, 9461. For examples of using 2,3-cyclic carbonates as glycosyl donors, see: (a) Gorin, P. A.; Perlin, A. S. Can. J. Chem. 1961, 39, 2474.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9461
-
-
Benakli, K.1
Zha, C.2
Kerns, R.J.3
-
14
-
-
0001023062
-
-
During the preparation of this manuscript, Kerns et al. reported the use of oxazolidinone protected glucosamine derivatives for the synthesis of α-linked 2-amino glycosides. Benakli, K.; Zha, C.; Kerns, R. J. J. Am. Chem. Soc. 2001, 123, 9461. For examples of using 2,3-cyclic carbonates as glycosyl donors, see: (a) Gorin, P. A.; Perlin, A. S. Can. J. Chem. 1961, 39, 2474.
-
(1961)
Can. J. Chem.
, vol.39
, pp. 2474
-
-
Gorin, P.A.1
Perlin, A.S.2
-
15
-
-
84988058248
-
-
(b) Betaneli, V. I.; Ovchinnikov, M. V.; Backinowsky, L. V.; Kochetkov, N. K. Carbohydr. Res. 1980, 84, 211.
-
(1980)
Carbohydr. Res.
, vol.84
, pp. 211
-
-
Betaneli, V.I.1
Ovchinnikov, M.V.2
Backinowsky, L.V.3
Kochetkov, N.K.4
-
16
-
-
0041720045
-
-
(c) Kochetkov, N. K.; Toroov, V. I.; Malysheva, N. N.; Shashkov, A. S. Tetrahedron 1980, 36, 1099.
-
(1980)
Tetrahedron
, vol.36
, pp. 1099
-
-
Kochetkov, N.K.1
Toroov, V.I.2
Malysheva, N.N.3
Shashkov, A.S.4
-
17
-
-
0034629293
-
-
(d) Crich, D.; Cai, W.; Dai, Z. J. Org. Chem. 2000, 65, 1291.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1291
-
-
Crich, D.1
Cai, W.2
Dai, Z.3
-
18
-
-
0002086064
-
-
Garegg, P. J.; Hultberg, H.; Wallin, S.; Carbohydr. Res. 1982, 108, 97.
-
(1982)
Carbohydr. Res.
, vol.108
, pp. 97
-
-
Garegg, P.J.1
Hultberg, H.2
Wallin, S.3
-
19
-
-
0025309559
-
-
(a) Konradsson, P.; Udodong, U. E.; Fraser-Reid, B. Tetrahedron Lett. 1990, 31, 4313.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 4313
-
-
Konradsson, P.1
Udodong, U.E.2
Fraser-Reid, B.3
|