Highly enantioselective sulfur ylide epoxidation reactions.
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Sulfide–BF3·OEt2 mediated Baylis–Hillman reactions
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A theoretical study of the reaction of alkynylboranes with butadiene: competition between cycloaddition and alkynylboration.
– The Journal of Organic Chemistry
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67,
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Effective chemical information.
– ABSTR PAP AM CHEM S
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A highly enantioselective one-pot sulfur ylide epoxidation reaction
– Tetrahedron Letters
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43,
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Nitrone cyclisations: the development of a semi-quantitative model from ab initio calculations
– Tetrahedron
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58,
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Theoretical studies of aldol stereoselectivity: the development of a force field model for enol borinates and the investigation of chiral enolate .pi.-face selectivity
– The Journal of Organic Chemistry
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55,
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SECONDARY STRUCTURAL INVESTIGATIONS OF NOVEL OXETANE AMINO ACID OLIGOMERS
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Sulfide/BF<sub>3</sub>.OEt<sub>2</sub> mediated Baylis-Hillman reactions:: What is the role of sulfur?
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223,
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Site-specific examination of secondary structure and orientation determination in membrane proteins: The peptidic13C?18O group as a novel infrared probe
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The stereochemistry of glabrescol
– Tetrahedron Letters
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42,
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Studies on the formation of a tricyclic c<inf>2</inf>-symmetric sulfide
– Tetrahedron Letters
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42,
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Gas phase versus solution chemistry: On the reversal of regiochemistry of methylation of sp<sup>2</sup>- and sp<sup>3</sup>-nitrogens
– Tetrahedron Letters
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42,
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Theoretical evaluation of the origin of the regio- and stereoselectivity in the Diels-Alder reactions of dialkylvinylboranes:: Studies on the reactions of vinylborane, dimethylvinylborane, and vinyl-9-BBN with <i>trans</i>-piperylene and isoprene
– Journal of the American Chemical Society
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Chemistry 2000: Resolving finer detail.
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Computational studies on the Diels-Alder reactions of vinyl- and alkynylboranes.
– ABSTR PAP AM CHEM S
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222,
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10-Helical conformations in oxetane beta-amino acid hexamers
– Tetrahedron Letters
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42,
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Novel inhibitors of Leishmanial dihydrofolate reductase
– Bioorg Med Chem Lett
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Stereocontrol in a one-pot procedure for anionic oxy-Cope rearrangement followed by intramolecular aldol reaction
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1051
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A Double Ring Closing Metathesis Reaction in the Rapid, Enantioselective Synthesis of NK-1 Receptor Antagonists
– Organic Letters
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