Synthesis of optically active aminooxy alcohols
Author:
Publisher
Elsevier BV
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Reference29 articles.
1. β-Amino alcohols from amino acids: Chelation control via schiff bases.
2. Preparation of protected amino aldehydes
3. Resolution of secondary alcohols using lipase in diisopropyl ether
4. Lipase-catalyzed kinetic resolution with in situ racemization: one-pot synthesis of optically active cyanohydrin acetates from aldehydes
5. N4-isopropyl-N-methyl formamidine, a reagent for the synthesis of bioactive amino-alcohols.
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1. Catalytic enantioselective dehydrogenative Si–O coupling of oxime ether-functionalized alcohols;Tetrahedron;2012-04
2. An Efficient One-Pot Synthesis of Oxime Ethers from Alcohols Using Triphenylphosphine/Carbon Tetrachloride;Synthesis;2010-03-24
3. Aqueous-Mediated Ring Opening of Epoxides with Oximes: A Rapid Entry into β-Hydroxy Oxime O-Ethers as Potential β-Adrenergic Blocking Agents;Synthesis;2008-06-11
4. Trends in lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds;Tetrahedron;2007-02
5. A simple and efficient synthesis of optically pure 4-alkylisoxazolidin-4-ols;Tetrahedron Letters;2006-10
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