☰

Tara R. Rheault, Ph.D. - Publications

Affiliations: 
2002 North Dakota State University, Fargo, ND, United States 
Area:
Synthetic Organic Chemistry, Natural Products
Tree Info Similar researchers PubMed Report error

9 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
2009 Rheault TR, Donaldson KH, Cheung M. Convenient synthesis of heteroaryl-linked benzimidazoles via microwave-assisted boronate ester formation Tetrahedron Letters. 50: 1399-1402. DOI: 10.1016/j.tetlet.2009.01.087  0.32
2004 Sibi MP, Patil K, Rheault TR. Synthesis of Oxacycles by Tandem Radical Addition-Cyclization Reactions European Journal of Organic Chemistry. 372-384. DOI: 10.1002/Ejoc.200300063  0.666
2004 Sibi MP, Zimmerman J, Rheault T. Enantioselective Conjugate Radical Addition to β-Acyloxy Acrylate Acceptors: An Approach to Acetate Aldol-Type Products. Cheminform. 35. DOI: 10.1002/chin.200403026  0.682
2003 Sibi MP, Zimmerman J, Rheault T. Enantioselective conjugate radical addition to β-acyloxy acrylate acceptors: An approach to acetate aldol-type products Angewandte Chemie - International Edition. 42: 4521-4523. PMID 14520755 DOI: 10.1002/Anie.200352096  0.629
2003 Rheault TR, Sibi MP. Radical-mediated annulation reactions Synthesis. 803-819. DOI: 10.1055/S-2003-38674  0.62
2002 Sibi MP, Rheault TR, Chandramouli SV, Jasperse CP. Acyclic diastereoselection in prochiral radical addition to prochiral olefins. Journal of the American Chemical Society. 124: 2924-30. PMID 11902883 DOI: 10.1021/Ja017510T  0.631
2001 Sibi MP, Chen J, Rheault TR. Radical-mediated annulation reactions. A versatile strategy for the preparation of a series of carbocycles Organic Letters. 3: 3679-3681. PMID 11700111 DOI: 10.1021/Ol016597K  0.65
2001 Sibi MP, Rheault TR, Miyabe H, Patil K, Jasperse CP. Highly diastereoselective radical addition-cyclization strategy: Facile synthesis of substituted furans Comptes Rendus De L'Academie Des Sciences - Series Iic: Chemistry. 4: 581-584. DOI: 10.1016/S1387-1609(01)01279-8  0.667
2000 Sibi MP, Rheault TR. Higher selectivity at higher temperatures! Effect of precursor stereochemistry on diastereoselectivity in radical allylations. Insight into the role of the Lewis acid Journal of the American Chemical Society. 122: 8873-8879. DOI: 10.1021/Ja001456J  0.592
Show low-probability matches.