Asymmetric hetero Diels-Alder reaction catalyzed by stable and easily prepared CAB catalysts
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (4), 979-988
- https://doi.org/10.1016/s0040-4020(01)80812-7
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Catalyzed Asymmetric SE′ Addition of Allylstannanes to AldehydesSynlett, 1992
- Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. The novel effect of the trialkysilyl group of the silyl ketene acetal on the reaction courseThe Journal of Organic Chemistry, 1991
- Catalytic asymmetric aldol reactions. Use of a chiral (acyloxy)borane complex as a versatile Lewis-acid catalystJournal of the American Chemical Society, 1991
- Asymmetric hetero Diels-Alder reactions catalyzed by novel chiral vanadium(IV) bis(1,3-diketonato) complexesOrganometallics, 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
- Chiral (acyloxy)borane (CAB): a powerful and practical catalyst for asymmetric Diels-Alder reactionsThe Journal of Organic Chemistry, 1989
- Electronic and Steric Effects of Lewis Acidic Organoaluminum Reagents in the Diels-Alder ReactionSynthetic Communications, 1988
- A fully synthetic route to hikosamineJournal of the American Chemical Society, 1985
- Derivatives of 1-methoxy-3-trimethylsilyloxy-1,3-butadiene for Diels-Alder reactionsJournal of the American Chemical Society, 1979