Abstract
A tetrahydrofuranyl β-amino acid has been prepared by using the asymmetric dihydroxylation of a furyl alkene to establish the stereochemistry. The furan moiety was employed as a carboxylic acid surrogate.
Original language | English |
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Article number | st-2015-d0655-l |
Pages (from-to) | 93-95 |
Number of pages | 3 |
Journal | Synlett |
Volume | 27 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 4 2016 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© Georg Thieme Verlag Stuttgart New York Synlett 2016.
ASJC Scopus Subject Areas
- Organic Chemistry
Keywords
- amino acid
- dihydroxylation
- furan
- oxidation
- tetrahydrofuran