Cyclization reactions of N-(2-chloroethylcarbamoyl) amino acids
β Scribed by H.S. Vargha; H. Medzihradszky-Schweiger; F. Ruff; K. Medzihrauszky
- Book ID
- 108372778
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 354 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4020
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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 βFull Textβ option. The original article is trackable v
Enantiomerically pure acetylene-containing aamino acids were used as versatile starting materials for the synthesis of a variety of heterocycles via Pd-mediated cyclization reactions. Depending on the protecting group strategy, both the carboxylate and the amine function of the amino acids could par
Acetylene-containing amino acids, obtained in enantiopure form via an enzymatic resolution process, serve as versatile intermediates in the synthesis of various highly functionalized heterocycles. The key transformations, intramolecular OC-and NC-bond formation, proceed via Pd-catalysis.