Biocatalytic asymmetric synthesis of β-aminoacid esters: improved chiral recognition in the presence of β-cyclodextrin
✍ Scribed by K.Rama Rao; Y.V.D. Nageswar; H.M.Sampath Kumar
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 124 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The radical polymerization of N-tert-butyl-N-allylacrylamide (t-BAA) was carried out in a dimethyl sulfoxide/H 2 O mixture in the presence of -cyclodextrin (-CD). The polymerization proceeded with the complete cyclization of the t-BAA unit and yielded optically active poly(t-BAA). The IR spectrum
The synthesis of enantiomerically enriched a-amino acids is described, by means of the diastereoselective conjugate addition of Grignard reagent to (S)-2-acetamidoacrylic ethoxycarbonylphenyl-methyl ester 1 and its N-Boo derivative 5 in the presence of Lewis acids. The addition of magnesium organocu
## Abstract For Abstract see ChemInform Abstract in Full Text.