STEREOSELECTIVE REDUCTION OF α-HYDROXY OXIME ETHERS: A CONVENIENT ROUTE TO CIS-1,2-AMINO ALCOHOLS
Overview
Authors
Affiliations
Reduction of cyclic α-hydroxyketoximes with borane provides an excellent, high yielding, regio- and stereoselective route to CIS-1, 2-amlnoalcohols.
Ghosh A, Mathivanan P, Cappiello J Tetrahedron Lett. 2018; 37(22):3815-3818.
PMID: 30411722 PMC: 6219759. DOI: 10.1016/0040-4039(96)00721-6.
-1-Aminoindan-2-ol in Asymmetric Syntheses.
Ghosh A, Fidanze S, Senanayake C Synthesis (Stuttg). 2018; 1998(7):937-961.
PMID: 30393403 PMC: 6214626. DOI: 10.1055/s-1998-2092.
Ghosh A, Duong T, McKee S J Chem Soc Chem Commun. 2018; 1992(22):1673-1674.
PMID: 30364406 PMC: 6196354. DOI: 10.1039/C39920001673.
Ghosh A, Liu W, Xu Y, Chen Z Angew Chem Int Ed Engl. 2018; 35(1):74-76.
PMID: 30344446 PMC: 6195359. DOI: 10.1002/anie.199600741.
Study of the Room-Temperature Synthesis of Oxime Ethers by using a Super Base.
Kosmalski T, Studzinska R, Daniszewska N, Ullrich M, Sikora A, Marszall M ChemistryOpen. 2018; 7(7):551-557.
PMID: 30065906 PMC: 6058178. DOI: 10.1002/open.201800098.