Chad Edward Bennett - Publications

Affiliations: 
2000 Indiana University, Bloomington, Bloomington, IN, United States 

15 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Roush WR, Narayan S, Bennett CE, Briner K. ChemInform Abstract: Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates. Cheminform. 30: no-no. DOI: 10.1002/chin.199948214  0.597
2010 Roush WR, Gung BW, Bennett CE. ChemInform Abstract: 2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides. Cheminform. 30: no-no. DOI: 10.1002/chin.199947217  0.507
2010 Roush WR, Bennett CE. ChemInform Abstract: A Highly Stereoselective Synthesis of 2-Deoxy-β-glycosides Using 2-Deoxy-2-iodo-glucopyranosyl Acetate Donors. Cheminform. 30: no-no. DOI: 10.1002/chin.199934229  0.524
2010 ROUSH WR, SEBESTA DP, BENNETT CE. ChemInform Abstract: 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. Cheminform. 28: no-no. DOI: 10.1002/chin.199744233  0.546
2006 Bennett CE, Figueroa R, Hart DJ, Yang D. Substituent effects on the regiochemical and stereochemical course of the nussbaumer-frater variation of the prins cyclization Heterocycles. 70: 119-128. DOI: 10.3987/Com-06-S(W)39  0.306
2003 Hart DJ, Bennett CE. Acid-promoted Prins cyclizations of enol ethers to form tetrahydropyrans. Organic Letters. 5: 1499-502. PMID 12713308 DOI: 10.1021/Ol0342756  0.452
2001 Roush WR, Bennett CE, Roberts SE. Studies on the synthesis of landomycin A: synthesis and glycosidation reactions of L-rhodinosyl acetate derivatives. The Journal of Organic Chemistry. 66: 6389-93. PMID 11559191 DOI: 10.1021/Jo015756A  0.527
2000 Roush WR, Bennett CE. A highly stereoselective synthesis of the landomycin a hexasaccharide unit [10] Journal of the American Chemical Society. 122: 6124-6125. DOI: 10.1021/Ja000743K  0.509
1999 Roush WR, Narayan S, Bennett CE, Briner K. Iodoacetoxylation of glycals using cerium(IV) ammonium nitrate, sodium iodide, and acetic acid: stereoselective synthesis of 2-deoxy-2-iodo-alpha-mannopyranosyl acetates. Organic Letters. 1: 895-7. PMID 10823219 DOI: 10.1021/Ol990815G  0.586
1999 Roush WR, Gung BW, Bennett CE. 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. Organic Letters. 1: 891-3. PMID 10823218 DOI: 10.1021/Ol9908070  0.485
1999 Roush WR, Bennett CE. A highly stereoselective synthesis of 2-deoxy-β-glycosides using 2- deoxy-2-iodo-glucopyranosyl acetate donors [7] Journal of the American Chemical Society. 121: 3541-3542. DOI: 10.1021/Ja984365J  0.549
1997 Roush WR, Sebesta DP, Bennett CE. Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 1. Stereochemistry of the reactions of d-glucal derivatives with phenylsulfenyl chloride and phenylselenenyl chloride Tetrahedron. 53: 8825-8836. DOI: 10.1016/S0040-4020(97)90394-X  0.519
1997 Roush WR, Sebesta DP, Bennett CE. Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 1. Stereochemistry of the reactions of D-glucal derivatives with phenylsulfenyl chloride and phenylselenenyl chloride Tetrahedron. 53: 8825-8836. DOI: 10.1016/S0040-4020(97)00571-1  0.423
1995 Marshall JA, Bennett CE. Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives. [Erratum to document cited in CA122:31231] The Journal of Organic Chemistry. 60: 2644-2644. DOI: 10.1021/Jo00113A060  0.313
1994 Marshall JA, Bennett CE. Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives The Journal of Organic Chemistry. 59: 6110-6113. DOI: 10.1021/Jo00099A054  0.342
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