Pamela J. Lombardi, Ph.D.
Affiliations: | 2001-2006 | Chemistry | Columbia University, New York, NY |
| 2006-2009 | Chemistry | Boston College, Newton, MA, United States | |
| 2009- | Chemistry | Stonehill College, Easton, MA, United States |
Area:
Organic synthesisGoogle:
"Pamela Lombardi"Mean distance: 7.83 | S | N | B | C | P |
Parents
Sign in to add mentor| David M. Lemal | research assistant | Dartmouth | ||
| James L. Leighton | grad student | 2006 | Columbia | |
| (Strained silacycles in the development of new asymmetric reactions.) | ||||
| Amir H. Hoveyda | post-doc | Boston College | ||
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Publications
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| Khan RK, Zhugralin AR, Torker S, et al. (2012) Synthesis, isolation, characterization, and reactivity of high-energy stereogenic-at-Ru carbenes: stereochemical inversion through olefin metathesis and other pathways. Journal of the American Chemical Society. 134: 12438-41 |
| Hoveyda AH, Lombardi PJ, O'Brien RV, et al. (2009) H-bonding as a control element in stereoselective Ru-catalyzed olefin metathesis. Journal of the American Chemical Society. 131: 8378-9 |
| Tran K, Lombardi PJ, Leighton JL. (2008) An efficient asymmetric synthesis of manzacidin C. Organic Letters. 10: 3165-7 |
| Shirakawa S, Lombardi PJ, Leighton JL. (2005) A simple and general chiral silicon Lewis acid for asymmetric synthesis: highly enantioselective [3+2] acylhydrazone-enol ether cycloadditions. Journal of the American Chemical Society. 127: 9974-5 |
| Shirakawa S, Lombardi PJ, Leighton JL. (2005) A simple and general chiral silicon Lewis acid for asymmetric synthesis: Highly enantioselective [3 + 2] acylhydrazone-enol ether cycloadditions Journal of the American Chemical Society. 127: 9974-9975 |
| Hackman BM, Lombardi PJ, Leighton JL. (2004) Highly diastereo- and enantioselective reagents for aldehyde crotylation Organic Letters. 6: 4375-4377 |
| Lombardi PJ, Gan Y, Lemal DM. (2002) Synthesis and chemistry of highly fluorinated oxepane-2,7-diols Collection of Czechoslovak Chemical Communications. 67: 1486-1492 |