syn‐Selective Michael Reaction of α‐Branched Aryl Acetaldehydes with Nitroolefins Promoted by Squaric Amino Acid Derived Bifunctional Brønsted Bases
Open Access
- 4 June 2021
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2021 (25), 3604-3612
- https://doi.org/10.1002/ejoc.202100355
Abstract
No abstract availableKeywords
Funding Information
- Euskal Herriko Unibertsitatea
- Eusko Jaurlaritza (IT1236-19)
This publication has 107 references indexed in Scilit:
- Recent Advances in Direct Catalytic Asymmetric Transformations under Proton‐Transfer ConditionsAngewandte Chemie, 2011
- Practical access to highly enantioenriched quaternary carbon Michael adducts using simple organocatalystsOrganic & Biomolecular Chemistry, 2010
- Prolylprolinol-Catalyzed Asymmetric Michael Addition of Aliphatic Aldehydes to NitroalkenesAdvanced Synthesis & Catalysis, 2010
- Squaramide‐Catalyzed Enantioselective Michael Addition of Diphenyl Phosphite to NitroalkenesAngewandte Chemie, 2009
- Chiral Squaramide Derivatives are Excellent Hydrogen Bond Donor CatalystsJournal of the American Chemical Society, 2008
- Water-Driven Chemoselective Reaction of Squarate Derivatives with Amino Acids and PeptidesOrganic Letters, 2007
- A Chiral Primary Amine Thiourea Catalyst for the Highly Enantioselective Direct Conjugate Addition of α,α‐Disubstituted Aldehydes to NitroalkenesAngewandte Chemie, 2006
- Squaric Acid-Based Peptidic Inhibitors of Matrix Metalloprotease-1The Journal of Organic Chemistry, 2005
- Enantio- and Diastereoselective Michael Reaction of 1,3-Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional ThioureaJournal of the American Chemical Society, 2004
- Aldol methodology: synthesis of versatile intermediates, 3-hydroxy-2-vinylcarbonyl compoundsJournal of the American Chemical Society, 1982