Tetrahedron Letters p. 9033 - 9036 (1996)
Update date:2022-08-03
Topics:
Weltering, Thomas J.
Weitz-Schmidt, Gabriele
Wong, Chi-Huey
The biological activity of a potent selectin antagonist could be 40-fold enhanced by attachment of a lipid moiety. Also an enantioselective synthesis of β,ω-dihydroxyamino acids by Sharpless asymmetric dihydroxylation (AD-reaction) allowed general access to this important class of compounds. Copyright (C) 1996 Elsevier Science Ltd.
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Doi:10.1016/S0040-4039(96)02034-5
(1996)Doi:10.1016/j.tet.2004.07.070
(2004)Doi:10.1039/DT9960004449
(1996)Doi:10.1016/S1872-2067(15)60896-8
(2015)Doi:10.1021/om960790e
(1997)Doi:10.1016/S0040-4039(01)98897-5
(1968)
