Cu(II)-Catalyzed Enantioselective Conjugate Reduction for the Synthesis ofN-Arylβ-Amino Acid Esters

Autor:	Jing Wu, Qiang Fang, Yi-Hu Hu, Hong-Feng Xia, Yao-Zong Sui, Shijun Li, Min Li
Rok vydání:	2012
Předmět:	chemistry.chemical_classification Reaction conditions Hydrosilylation Stereochemistry Aryl Enantioselective synthesis chemistry.chemical_element General Chemistry Copper Amino acid Catalysis chemistry.chemical_compound chemistry Conjugate
Zdroj:	Chinese Journal of Chemistry.
ISSN:	1001-604X
Popis:	A new set of reaction conditions has been established and allowed for the first non-noble Cu(II)-catalyzed asymmetric 1,4-hydrosilylation of N-aryl β-enamino esters under air to afford a selection of N-aryl β-amino acid esters of moderate-to-good enantiopurities (ee up to 91%).
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3e2333847ba7ca756d383576e54ffa7c https://doi.org/10.1002/cjoc.201200779 Zobrazit plný text záznamu Plný text