Catalytic, enantioselective alkylations of N,O- and N,N-acetals and hemiacetals

Citation
D. Ferraris et al., Catalytic, enantioselective alkylations of N,O- and N,N-acetals and hemiacetals, TETRAHEDRON, 55(29), 1999, pp. 8869-8882
Citations number
41
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
29
Year of publication
1999
Pages
8869 - 8882
Database
ISI
SICI code
0040-4020(19990716)55:29<8869:CEAONA>2.0.ZU;2-A
Abstract
We report the first examples of catalytic, enantioselective alkylation of N ,O-acetals to produce useful amino acid derivatives 5 in high yield (73-93% ) and enantioselectivity (70-96%). We have extended the utility of our reac tion to include a simple one-pot procedure from readily available starting materials. We also provide several different N-based protecting groups that greatly increase the flexibility of the reaction. In addition, we have elu cidated novel mechanistic information including the discovery of unique tra nsilylations that start off the catalytic reactions of enol silane nucleoph iles with N,O-acetals. These details will guide us in further explorations of the reaction's scope and utility. (C) 1999 Elsevier Science Ltd. All rig hts reserved.