Tetrahedron Letters p. 2101 - 2104 (1990)
Update date:2022-08-02
Topics:
Corcoran, Robert C.
Regioselectivity in the cleavage of chiral 2-substituted-3-methoxymethyl-1,3-dioxanes can be controlled to a high degree by choice of an appropriate activating Lewis acid.However, the diastereoselectivity of the cleavage reactions is uniformely poor.
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Doi:10.1021/jo00197a045
(1984)Doi:10.1016/0040-4020(94)01039-3
(1995)Doi:10.1016/j.bmcl.2010.11.108
(2011)Doi:10.1021/jo00312a015
(1990)Doi:10.1016/j.bmc.2011.03.006
(2011)Doi:10.1016/S0040-4039(00)97585-3
(1990)
