Preparation of an electrophilic glycine cation equivalent and its reaction with heteroatom nucleophiles
β Scribed by Martin J. O'Donnell; William D. Bennett; Robin L. Polt
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 229 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A variety of heteroatom substituted Schiff base amino esters 4 -1 are prepared either from the benzophenone imine of glycine ethyl ester (1) or by reaction of acetate 4 with heteroatom nucleophiles.
π SIMILAR VOLUMES
## 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 βFull Textβ option. The original article is trackable v
A simple and general synthesis of a-amino acids employing vinyl and alkyl Grignard reagents with a glycine cation equivalent is described. B,v-Unsaturated a-amino acids are natural products that possess antibiotic activity and enzyme inhibitory properties. 3 Several synthetic B,T-unsaturated a-amino