Tetrahedron Letters p. 5181 - 5184 (1997)
Update date:2022-08-05
Topics:
Hashimoto, Shun-Ichi
Sakamoto, Hiroki
Honda, Takeshi
Ikegami, Shiro
Efficient synthetic strategy for oligosaccharides has been developed by exploiting the difference in anomeric reactivity between glycosyl donors and acceptors carrying phosphorus-containing leaving groups, wherein, the tetramethylphosphoroamidate group plays a pivotal role as anomeric protective group as well as leaving group.
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Doi:10.1246/cl.1997.801
(1997)Doi:10.1016/0040-4039(93)88091-V
(1993)Doi:10.1016/S0040-4039(97)01242-2
(1997)Doi:10.1021/jo9706842
(1997)Doi:10.1016/S0020-1693(96)05583-1
(1997)Doi:10.1021/jo970237m
(1997)
