Enantioselective Synthesis of α-Amino Acids from Nitroalkenes. -Careful oxidation of the addition products (I) of (R)-4-phenyl-2-oxazolidine and nitroalkenes yields the acids (II) which can be easily cleaved to D-α-amino acids of high optical purity.
ChemInform Abstract: Enantioselective Synthesis of α,α-Disubstituted Amines from Nitroalkenes.
✍ Scribed by Mary-Lorene Leroux; Thierry Le Gall; Charles Mioskowski
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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 via the “References” option.
📜 SIMILAR VOLUMES
## Abstract An epi‐quinine derivative ACI is found to be an efficient catalyst for the synthesis of α‐hydrazino aldehydes.
## Abstract The formation of the desired products is accompanied by little or trace amounts of linear amines such as (IV).
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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