Asymmetric synthesis of α,α-disubstituted α-amino acid derivatives using MABR promoted rearrangement
✍ Scribed by Masayuki Matsushita; Hana Maeda; Mitsuaki Kodama
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 211 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
An efficient route for the asymmetric synthesis of ct,a-disubstituted or-amino acids derivatives (1, 2, and 3) starting from readily available epoxy silyl ethers (6) has been developed. High enantiomeric purity can be realized by the present method using a combination of MABR rearrangement of a chiral epoxide and Curtius rearrangement.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
Copper(salen) complex 1 has been found to catalyse the asymmetric alkylation of enolates derived from a variety of amino acids. There is a clear relationship between the size of the side chain in the substrate and the enantioselectivity of the process, so that the enantioselectivity decreases in the
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v