ChemInform Abstract: Asymmetric Reduction of Keto Oxime Ethers Using Oxazaborolidine Reagents. The Enantioselective Synthesis of Cyclic Amino Alcohols

Autor:	Ulf H. Dolling, Paul J. Reider, D. M. Tschaen, R. D. Tillyer, Charles Boudreau
Rok vydání:	2010
Předmět:	Reduction (complexity) chemistry.chemical_compound chemistry Reagent Enantioselective synthesis General Medicine Oxime Combinatorial chemistry Catalysis
Zdroj:	ChemInform. 26
ISSN:	0931-7597
DOI:	10.1002/chin.199540117
Popis:	Asymmetric reduction of keto oxime ethers 2 catalyzed by oxazaborolidine-borane complex 4 produces the cis amino alcohols 1 efficiently and with high levels of diastereo- and enantioselectivity.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::33e6422d0a55c7ce11e787e9be5adba4 https://doi.org/10.1002/chin.199540117 Zobrazit plný text záznamu Plný text