Enantioselective synthesis of D-erythro-sphingosine

B Bernet, A Vasella

Index: Bernet, Bruno; Vasella, Andrea Tetrahedron Letters, 1983 , vol. 24, # 49 p. 5491 - 5494

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Citation Number: 77

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... D-erythro-sphingosine ( ) and the 3-amino-2-hydroxy-L-erythro isomer were synthesized in a highly enantio- and regioselective manner by a modified Sharpless asymmetric epoxidation. ... The reaction proceeded noticeably slower than a similar epoxidation of geraniol.