A short enantioselective synthesis of N-Boc-α-amino acids from epoxy alcohols
- 1 November 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (48) , 7781-7784
- https://doi.org/10.1016/s0040-4039(00)61565-4
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- A general, catalytic, and enantioselective synthesis of .alpha.-amino acidsJournal of the American Chemical Society, 1992
- Regioselective ring opening of chiral epoxyalcohols by primary aminesTetrahedron Letters, 1991
- A Mild and Efficient Sonochemicaltert-Butoxycarbonylation of Amines from Their SaltsSynlett, 1991
- An improved synthesis of the taxol side chain and of RP 56976The Journal of Organic Chemistry, 1990
- One-pot transformation of azido-group to N-(t-butoxycarbonyl)amino groupTetrahedron Letters, 1989
- Regioselective azide opening of 2,3-epoxy alcohols by [Ti(O-i-Pr)2(N3)2]: synthesis of .alpha.-amino acidsThe Journal of Organic Chemistry, 1988
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- Absolute configuration of 2-amino-4-phenyl butyric acidThe Journal of Organic Chemistry, 1982
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- A new class of angiotensin-converting enzyme inhibitorsNature, 1980