Synthesis of enantiomerically enriched secondary and tertiary phenylthio- and phenoxy-aldols

BERNARD, ANGELA MARIA;FRONGIA, ANGELO;SECCI, FRANCESCO;
2008-01-01

Abstract

alpha-Phenoxy- and phenylthio-ketones have been explored as donors and acceptors in organocatalytic aldol reactions. Our studies have revealed effective methodologies for accessing structurally varied and enantiomerically enriched secondary and tertiary phenylthio- and phenoxy-aldols, expanding the scope and potential synthetic utility of organocatalytic direct aldol reactions. (C) 2008 Elsevier Ltd. All rights reserved.
2008
TETRAHEDRON LETTERS
49
19
3037
3041
5
WOS:000255774700001
2-s2.0-41749109302
Bernard, ANGELA MARIA; Frongia, Angelo; Piras, Pp; Secci, Francesco; Spiga, M.
1.1 Articolo in rivista
info:eu-repo/semantics/article
1 Contributo su Rivista::1.1 Articolo in rivista
262
5
none
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