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Chad E. Bennett

Indiana University Bloomington

16

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Stereoselective Synthesis of 2-Deoxy-β-glycosides from Glycal Precursors. Part 1. Stereochemistry of the Reactions of D-Glucal Derivatives with Phenylsulfenyl Chloride and Phenylselenenyl Chloride.

2010 ChemInform
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Acid-Promoted Prins Cyclizations of Enol Ethers To Form Tetrahydropyrans

2003 Organic Letters
- David J. Hart
- Chad E. Bennett
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HIGHLY STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA-GLYCOSIDES. APPLICATION TO THE TOTAL SYNTHESIS OF LANDOMYSIN A

2002
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The practical synthesis of a novel and highly potent analogue of bryostatin.

2002 Journal of the American Chemical Society
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Studies on the Synthesis of Landomycin A: Synthesis and Glycosidation Reactions of l-Rhodinosyl Acetate Derivatives

2001 Journal of Organic Chemistry
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A Highly Stereoselective Synthesis of the Landomycin A Hexasaccharide Unit

2000 Journal of the American Chemical Society
- William R. Roush
- Chad E. Bennett
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A HIGHLY STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA -GLYCOSIDES USING 2-DEOXY-2-IODO-GLUCOPYRANOSYL ACETATE DONORS

1999 Journal of the American Chemical Society
- William R. Roush
- Chad E. Bennett
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2-Deoxy-2-iodo- and 2-deoxy-2-bromo-alpha-glucopyranosyl trichloroacetimidates: highly reactive and stereoselective donors for the synthesis of 2-deoxy-beta-glycosides.

1999 Organic Letters
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Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates

1999 Organic Letters
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2-Deoxy-2-iodo- and 2-deoxy-2-bromo-alpha-glucopyranosyl trichloroacetimidates: highly reactive and stereoselective donors for the synthesis of 2-deoxy-beta-glycosides.

1999 Organic Letters
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Citations (39)