Diastereoselective conjugate addition of Grignard reagents to a homochiral fumaramide derived from Oppolzer’s sultam
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference21 articles.
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3. Influence ofLewis Acids on the [4 + 2] Cycloaddition ofN,N?-Fumaroylbis[(2R)-bornane-10,2-sultam] to Cyclopentadiene and application to various dienes
4. Camphor-DerivedN-Acryloyl andN-Crotonoyl Sultams: Practical Activated Dienophiles in AsymmetricDiels-alder Reactions. Preliminary Communication
5. Influence of the Solvent Polarity on the Stereoselectivity of the Uncatalyzed [4+2] Cycloaddition of Cyclopentadiene toN,N′-Fumaroyldi[(2R)-borane-10,2-sultam]
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1. Betti's base for crystallization-induced deracemization of substituted aldehydes: synthesis of enantiopure amorolfine and fenpropimorph;Organic & Biomolecular Chemistry;2017
2. Grignard1,4-Additions topara-Substituted (2R)-N-Cinnamoylbornane-10,2-sultam Derivatives: Revised Configuration for the N,OAc-Keteneacetal Formation in the Presence of Cu(I);Helvetica Chimica Acta;2016-07-06
3. Recent advances in the application of the Oppolzer camphorsultam as a chiral auxiliary;Tetrahedron: Asymmetry;2014-08
4. Conjugate Addition II;Key Chiral Auxiliary Applications;2014
5. Conjugate Addition Reactions of N-Carbamoyl-4-pyridones and 2,3-Dihydropyridones with Grignard Reagents in the Absence of Cu(I) Salts;The Journal of Organic Chemistry;2013-08-13
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