Stereoselective reduction of α-hydroxy oxime ethers: a convenient route to cis1,2-amino alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Stereochemical studies of adrenergic drugs. Diastereomeric 2-amino-1-phenylcyclobutanols
2. Synthesis and Absolute Configurations of Hexahydro-Naphthoxazines as Rigid Congeners of Phenmetrazine
3. Diastereoselective alkylation of the dianion of 5-ethoxy-4(S)-hydroxy-1-isopropyl-2-pyrrolidinone; Synthesis of enantiomerically pure azabicycles
4. Stereoselective conversion of valienamine and validamine into valiolamine
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3. Study of the Room-Temperature Synthesis of Oxime Ethers by using a Super Base;ChemistryOpen;2018-07
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5. Catalytic α-hydroxylation of ketones under CuBr2 or HBr/DMSO systems;Tetrahedron;2015-05
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