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- W2952393208 abstract "Enantiomerically pure acetylene-containing - amino 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 participate in the cyclizations, thus giving rise to oxygen heterocycles (-aminolactones) and nitrogen heterocycles (cyclic -amino acid derivatives), respectively. Beside the straightforward cyclization, cyclization/cross- coupling reactions were also successfully carried out to provide the corresponding substituted cyclic amino acid derivatives." @default.
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- W2952393208 date "2010-05-20" @default.
- W2952393208 modified "2023-09-24" @default.
- W2952393208 title "ChemInform Abstract: Palladium-Catalyzed Cyclization Reactions of Acetylene-Containing Amino Acids." @default.
- W2952393208 cites W1974199301 @default.
- W2952393208 doi "https://doi.org/10.1002/chin.200230227" @default.
- W2952393208 hasPublicationYear "2010" @default.
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