Highly Diastereoselective Diels−Alder Reaction Using a Chiral Auxiliary Derived from Levoglucosenone (original) (raw)
A chiral auxiliary derived from levoglucosenone in asymmetric Diels–Alder transformations
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Tetrahedron Letters, 2005
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2012
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Stacking Effect on Levoglucosenone Derived Internal Chiral Auxiliaries. A Case of Complete Enantioselectivity Inversion on the Diels−Alder Reaction
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Joseph Rico
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Camphor-DerivedN-Acryloyl andN-Crotonoyl Sultams: Practical Activated Dienophiles in AsymmetricDiels-alder Reactions. Preliminary Communication
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Tetrahedron: Asymmetry, 2000
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π-Stacking Effect on Levoglucosenone Derived Internal Chiral Auxiliaries. A Case of Complete Enantioselectivity Inversion on the Diels−Alder Reaction
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Single and double asymmetric induction in Diels-Alder cycloadditions with chiral acylnitroso dienophiles
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Asymmetric diels-alder reactions of acrylates derived from 3-alkyl-borneols and -isoborneols
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First Diels-Alder Reactions of Enantiomerically Pure 1-p-Tolylsulfinyl Dienes: Straightforward Access to Cyclohexenols through Tandem Cycloaddition/[2,3]-Sigmatropic Rearrangement
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Recent Applications of Levoglucosenone as Chiral Synthon
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Diastereofacial selectivity in Diels-Alder cycloadditions of methyl acrylate to facially differentiated unsymmetrical Cyclohexa-1,3-dienes
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Unexpectedly high diastereomeric induction in the diels-alder reaction of quinones with chiral aryl containing 1-alkoxy-3-trimethylsilyloxybuta-1,3-dienes
Jean-Paul Seerden
Tetrahedron Letters, 1990
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