Timothy A. Boebel, Ph.D. - Publications
Affiliations: | 2005 | University of Illinois, Urbana-Champaign, Urbana-Champaign, IL |
Area:
Organic Chemistry, Natural Product Synthesis, Medicinal ChemistryYear | Citation | Score | |||
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2010 | Robbins DW, Boebel TA, Hartwig JF. Iridium-catalyzed, silyl-directed borylation of nitrogen-containing heterocycles. Journal of the American Chemical Society. 132: 4068-9. PMID 20199022 DOI: 10.1021/Ja1006405 | 0.409 | |||
2008 | Boebel TA, Hartwig JF. Silyl-directed, iridium-catalyzed ortho-borylation of arenes. A one-pot ortho-borylation of phenols, arylamines, and alkylarenes. Journal of the American Chemical Society. 130: 7534-5. PMID 18494474 DOI: 10.1021/Ja8015878 | 0.464 | |||
2008 | Boebel TA, Hartwig JF. Iridium-catalyzed preparation of silylboranes by silane borylation and their use in the catalytic borylation of arenes Organometallics. 27: 6013-6019. DOI: 10.1021/Om800696D | 0.542 | |||
2008 | Boebel TA, Hartwig JF. Conversion of 1,3-disubstituted arenes to chiral α,α-diaryl methylammonium chlorides using arene borylation Tetrahedron. 64: 6824-6830. DOI: 10.1016/J.Tet.2008.04.060 | 0.352 | |||
2005 | Boebel TA, Gin DY. Probing the mechanism of sulfoxide-catalyzed hemiacetal activation in dehydrative glycosylation. The Journal of Organic Chemistry. 70: 5818-26. PMID 16018673 DOI: 10.1021/Jo050294C | 0.47 | |||
2003 | Boebel TA, Gin DY. Sulfoxide covalent catalysis: application to glycosidic bond formation. Angewandte Chemie (International Ed. in English). 42: 5874-7. PMID 14673924 DOI: 10.1002/Anie.200352761 | 0.443 | |||
2001 | Davies HML, Boebel TA. ChemInform Abstract: Asymmetric Synthesis of 1-Alkynylcyclopropane-1-carboxylates. Cheminform. 32: no-no. DOI: 10.1002/chin.200103084 | 0.306 | |||
2000 | Davies HM, Boebel TA. Asymmetric synthesis of 1-alkynylcyclopropane-1-carboxylates Tetrahedron Letters. 41: 8189-8192. DOI: 10.1016/S0040-4039(00)01453-2 | 0.396 | |||
2000 | Davies HML, Boebel TA. Asymmetric synthesis of 1-alkynylcyclopropane-1-carboxylates Tetrahedron Letters. 41: 8189-8192. | 0.313 | |||
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