Practical Synthesis of Enantiopure Cyclic 1,2-Amino Alcohols via Catalytic Asymmetric Ring Opening of Meso Epoxides
- 13 June 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (12) , 4197-4199
- https://doi.org/10.1021/jo970146p
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Synthesis of sialyl Lewis X mimetics: Use of O-α-fucosyl-(1R, 2R)-2-aminocyclohexanol as core structureTetrahedron Letters, 1996
- Application of indane-derived C2-symmetric bis(oxazolines) in two-point binding asymmetric Diels-Alder reactionsTetrahedron Letters, 1996
- Efficient Synthesis of (R)-4-((Trimethylsilyl)oxy)-2-cyclopentenone by Enantioselective Catalytic Epoxide Ring OpeningThe Journal of Organic Chemistry, 1996
- On the Mechanism of Asymmetric Nucleophilic Ring-Opening of Epoxides Catalyzed by (Salen)CrIII ComplexesJournal of the American Chemical Society, 1996
- Highly Enantioselective Ring Opening of Epoxides Catalyzed by (salen)Cr(III) ComplexesJournal of the American Chemical Society, 1995
- New chiral building blocks and their application to the construction of chiral aminoalcohols: Enantiomerically pure cis- and trans-3-mesyloxy-4-hydroxy tetrahydrofuransTetrahedron Letters, 1993
- The biosynthesis of spermidine. Part 3: the stereochemistry of the formation of the N-CH2 group in the biosynthesis of spermidineJournal of the Chemical Society, Perkin Transactions 1, 1985
- Reaction of trans-2-Acylaminocyclanols with Thionyl ChlorideCanadian Journal of Chemistry, 1971