Michael J. Lawler, Ph.D. - Publications
Affiliations: | 2008 | Chemistry | Indiana University, Bloomington, Bloomington, IN, United States |
Area:
Organic ChemistryYear | Citation | Score | |||
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2016 | Evans PA, Čusak A, Grisin A, Lawler MJ, Pink M. Medium-Ring Stereocontrol in the Temporary Silicon-Tethered Ring-Closing Metathesis Approach to the Synthesis of Polyketide Fragments Synthesis (Germany). 48: 2402-2412. DOI: 10.1055/S-0035-1562094 | 0.43 | |||
2012 | Evans PA, Huang MH, Lawler MJ, Maroto S. Total synthesis of marinomycin A using salicylate as a molecular switch to mediate dimerization. Nature Chemistry. 4: 680-4. PMID 22824902 DOI: 10.1038/Nchem.1330 | 0.447 | |||
2012 | Evans PA, Grisin A, Lawler MJ. Diastereoselective construction of syn-1,3-dioxanes via a bismuth-mediated two-component hemiacetal/oxa-conjugate addition reaction. Journal of the American Chemical Society. 134: 2856-9. PMID 22296255 DOI: 10.1021/Ja208668U | 0.476 | |||
2012 | Evans PA, Clizbe EA, Lawler MJ, Oliver S. Enantioselective rhodium-catalyzed allylic alkylation of acyclic α-alkoxy substituted ketones using a chiral monodentate phosphite ligand Chemical Science. 3: 1835-1838. DOI: 10.1039/C2Sc20141K | 0.516 | |||
2006 | Evans PA, Lawler MJ. Rhodium-catalyzed propargylic substitution: a divergent approach to propargylic and allenyl sulfonamides. Angewandte Chemie (International Ed. in English). 45: 4970-2. PMID 16819738 DOI: 10.1002/Anie.200600615 | 0.503 | |||
2006 | Denmark SE, Fu J, Lawler MJ. Chiral phosphoramide-catalyzed enantioselective addition of allylic trichlorosilanes to aldehydes. Preparative studies with bidentate phosphorus-based amides. The Journal of Organic Chemistry. 71: 1523-36. PMID 16468801 DOI: 10.1021/Jo052203H | 0.399 | |||
2004 | Evans PA, Lawler MJ. Regio- and diastereoselective rhodium-catalyzed allylic substitution with acyclic alpha-alkoxy-substituted copper(I) enolates: stereodivergent approach to 2,3,6-trisubstituted dihydropyrans. Journal of the American Chemical Society. 126: 8642-3. PMID 15250703 DOI: 10.1021/Ja049080N | 0.526 | |||
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