Organocatalytic Asymmetric Domino Knoevenagel/Diels–Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane‐1,5,9‐triones
- 15 September 2003
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 115 (35), 4365-4369
- https://doi.org/10.1002/ange.200351916
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Organocatalytic Asymmetric Conjugate Addition of Nitroalkanes to α,β-Unsaturated Enones Using Novel Imidazoline CatalystsThe Journal of Organic Chemistry, 2002
- The Enantioselective Organocatalytic 1,4-Addition of Electron-Rich Benzenes to α,β-Unsaturated AldehydesJournal of the American Chemical Society, 2002
- A Highly Enantioselective Amino Acid-Catalyzed Route to Functionalized α-Amino AcidsJournal of the American Chemical Society, 2002
- A Highly Enantioselective Route to Either Enantiomer of Both α- and β-Amino Acid DerivativesJournal of the American Chemical Society, 2002
- A Novel Proline-Catalyzed Three-Component Reaction of Ketones, Aldehydes, and Meldrum's AcidSynlett, 2001
- Domino Reactions in Organic SynthesisChemical Reviews, 1996
- Catalytic asymmetric Diels Alder reactionsChemical Reviews, 1992
- Stereochemical Behavior of Intermediary Compounds in the Amine-Catalyzed Knoevenagel ReactionBulletin of the Chemical Society of Japan, 1988
- Meldrum's acid in organic synthesis. V. Versatile one-pot synthesis of indolepropionic esters via simultaneous condensation of three different carbon components, indole, aldehydes and Meldrum's acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial StructuresAngewandte Chemie International Edition in English, 1971