Ming He, Ph.D. - Publications
Affiliations: | 2007 | Chemistry | University of California, Santa Barbara, Santa Barbara, CA, United States |
Area:
natural product total synthesisYear | Citation | Score | |||
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2013 | He M, Bode JW. E pluribus unum: Isolation, structure determination, network analysis and DFT studies of a single metastable structure from a shapeshifting mixture of 852 bullvalene structural isomers Organic and Biomolecular Chemistry. 11: 1306-1317. PMID 23188211 DOI: 10.1039/C2Ob26954F | 0.433 | |||
2012 | He M, Rommel M, Bode JW. Formal synthesis of (±)-clausenamide by nhc-catalyzed γ-lactam formation Heterocycles. 86: 1689-1696. DOI: 10.3987/Com-12-S(N)128 | 0.494 | |||
2011 | He M, Bode JW. Racemization as a stereochemical measure of dynamics and robustness in shape-shifting organic molecules. Proceedings of the National Academy of Sciences of the United States of America. 108: 14752-6. PMID 21873220 DOI: 10.1073/Pnas.1108170108 | 0.431 | |||
2008 | He M, Beahm BJ, Bode JW. Chiral NHC-catalyzed oxodiene Diels-Alder reactions with α-chloroaldehyde bisulfite salts Organic Letters. 10: 3817-3820. PMID 18656948 DOI: 10.1021/Ol801502H | 0.575 | |||
2008 | He M, Bode JW. Enantioselective, NHC-catalyzed bicyclo-β-lactam formation via direct annulations of enals and unsaturated N-sulfonyl ketimines Journal of the American Chemical Society. 130: 418-419. PMID 18092785 DOI: 10.1021/Ja0778592 | 0.537 | |||
2006 | He M, Uc GJ, Bode JW. Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene diels-alder reactions with low catalyst loadings Journal of the American Chemical Society. 128: 15088-15089. PMID 17117850 DOI: 10.1021/Ja066380R | 0.593 | |||
2006 | He M, Struble JR, Bode JW. Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes. Journal of the American Chemical Society. 128: 8418-20. PMID 16802805 DOI: 10.1021/Ja062707C | 0.636 | |||
2005 | He M, Bode JW. Catalytic Synthesis of gamma-Lactams via direct annulations of enals and N-sulfonylimines. Organic Letters. 7: 3131-4. PMID 15987223 DOI: 10.1021/Ol051234W | 0.577 | |||
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