Asymmetric diels-alder reactions catalyzed by chiral oxazaborolidines. Effect of the position of an electron-donor functionality in the α-side chain substituent on the enantioselectivity
- 16 April 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (16) , 2669-2672
- https://doi.org/10.1016/s0040-4039(00)77652-0
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studiesJournal of the American Chemical Society, 1992
- Catalytic asymmetric Diels Alder reactionsChemical Reviews, 1992
- Oxazaborolidine und Dioxaborolidine in der enantioselektiven Katalyse0Angewandte Chemie, 1992
- Enantioselective Diels-Alder reactions of enals: Fighting species multiplicity of the catalyst with donor solventsTetrahedron: Asymmetry, 1991
- Diels-Alder reactions with dienes bearing a remote stereogenic center. Conformational model for diastereofacial selectivityTetrahedron: Asymmetry, 1991
- The Efficient Catalytic Asymmetric Aldol-type ReactionChemistry Letters, 1990
- Asymmetric Synthesis Utilizing External Chiral LigandsSynthesis, 1990
- Enantioselective Diels-Alder Additions with New Chiral Lewis Acids Derived from Amino AcidsSynlett, 1990
- New Chiral Lewis Acid Catalysts Prepared from Simple Amino Acids and Their Use in Asymmetric Diels-Alder ReactionsSynlett, 1990
- Asymmetric Diels–Alder reaction catalysed by chiral alkoxyaluminium dichlorideJournal of the Chemical Society, Chemical Communications, 1979