## 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
Synthesis of novel amino acids, l-bis-tetrahydrofuranylglycines
β Scribed by Ei'ichi Ami; S Rajesh; Jung Wang; Tooru Kimura; Yoshio Hayashi; Yoshiaki Kiso; Toshimasa Ishida
- Book ID
- 104250871
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 138 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Novel amino acids, enantiomerically pure L-bis-tetrahydrofuranylglycines, were efficiently synthesized from dihydrofuran utilizing radical cyclization and chiral azidation as the key steps. The absolute stereochemistry of both diastereomers has been ascertained by their crystal structures.
π SIMILAR VOLUMES
Radicals generated by photofysis YW light1 of suitubly protected amino-acid derivutives of ~-hydroxy-~-thjopyr~done add efficientiy to o&voted olefins to offord ?otisfoctory yields of adducts, Ox~datiun of the thjopyridy~ residue to sulphoxide and thermol e~iminotion afford excellent yidds of the co