Stereocontrolled ‘one pot’ organometallic addition–ring opening reaction of α,β-aziridine aldehydes. A new entry to syn 1,2-amino alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Diastereo- and Enantioselective Synthesis of Vicinal Amino Alcohols by Oxa Michael Addition ofN-Formylnorephedrine to Nitro Alkenes
2. N-Diphenylmethylene-protected glycosyl acceptors. Selective β-O-glycosylation to form lactosyl-threo-ceramides
3. Halocyclization and Palladium(II)-Catalyzed Amidocarbonylation of Unsaturated Aminopolypols. Synthesis of 1,4-Iminoglycitols as Potential Glycosidase Inhibitors
4. Novel, Stereoselective Synthesis of 2-Amino Saccharides
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1. Two (Chemo)-Enzymatic Cascades for the Production of Opposite Enantiomers of Chiral Azidoalcohols;Catalysts;2021-08-17
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3. Nucleophilic ring opening of trans-2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity;Chemical Communications;2018
4. A new amino alcohol NpyNimineNamineOalcohol-donor ligand: coordination toward zinc(II) and cadmium(II) halides and enantioselective products;Journal of Coordination Chemistry;2017-10-10
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