Optically active 3-fluoro+lactam (1) was stereoselectively synthesized by the ketene-imine condensation method. Use of (1) in alkylation and aldol reactions resulted in the stereoselective formation of ( 2) and ( 3) respectively, but the control of the hydroxylated stereocenter was not possible in
Biocatalysis for the preparation of optically active β-lactam precursors of amino acids
✍ Scribed by Péter Csomós; Liisa T. Kanerva; Gábor Bernáth; Ferenc Fülöp
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 351 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0957-4166
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## 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
B-Amino acids2) are of great current interest because of their naturally occurring as the component of biologically active peptide antibiotics and also their structual relationship to the B-lactam, one of the most biologically important functional groups. We wish to describe here the catalytic asym
## Abstract For Abstract see ChemInform Abstract in Full Text.
## 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