Pd-Catalyzed cyclization reactions of acetylene-containing α-amino acids
✍ Scribed by Larissa B. Wolf; Kim C.M.F. Tjen; Floris P.J.T. Rutjes; Henk Hiemstra; Hans E. Schoemaker
- Book ID
- 104259436
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 335 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
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.
📜 SIMILAR VOLUMES
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
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