An efficient protocol for regioselective ring opening of epoxides using samarium triflate: Synthesis of propranolol, atenolol and RO363
- 11 September 2006
- journal article
- research article
- Published by Elsevier in Journal of Molecular Catalysis A: Chemical
- Vol. 261 (2) , 207-212
- https://doi.org/10.1016/j.molcata.2006.07.059
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- An efficient asymmetric synthesis of (S)-atenolol: using hydrolytic kinetic resolutionBioorganic & Medicinal Chemistry, 2005
- An efficient method for the ring opening of epoxides with aromatic amines catalyzed by bismuth trichlorideTetrahedron Letters, 2002
- The Synthesis of Vicinal Amino AlcoholsTetrahedron, 2000
- re- andsi-Face-Selective Nitroaldol Reactions Catalyzed by a Rigid Chiral Quaternary Ammonium Salt: A Highly Stereoselective Synthesis of the HIV Protease Inhibitor Amprenavir (Vertex 478)Angewandte Chemie International Edition in English, 1999
- Sharpless Asymmetric Aminohydroxylation: Scope, Limitations, and Use in SynthesisAngewandte Chemie International Edition in English, 1999
- Enantioselective desymmetrisation of achiral epoxidesTetrahedron, 1996
- 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric SynthesisChemical Reviews, 1996
- The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcoholsChemical Reviews, 1991
- Ultra-short-acting .beta.-adrenergic receptor blocking agents. 2. (Aryloxy)propanolamines containing esters on the aryl functionJournal of Medicinal Chemistry, 1982
- 1,2,3-oxathiazolidines. Heterocyclic systemThe Journal of Organic Chemistry, 1969