Jonathan K. Lam, Ph.D.
Affiliations: | 2014 | Chemistry | University of California, Irvine, Irvine, CA |
Area:
Organic and SyntheticGoogle:
"Jonathan Lam"Parents
Sign in to add mentorJin-Quan Yu | grad student | 2007-2010 | Scripps Institute | |
Christopher D. Vanderwal | grad student | 2014 | UC Irvine | |
(Part I: Ring-Rearrangement Metathesis of Himbert Arene-Allene Cycloadducts for the Rapid, Modular Construction of Complex Molecular Scaffolds. Part II: Application of Zincke Aldehydes Toward the Synthesis of Gelsemine.) | ||||
Richard Royce Schrock | post-doc | 2014-2016 | MIT |
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Publications
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Koh MJ, Nguyen TT, Lam JK, et al. (2017) Molybdenum chloride catalysts for Z-selective olefin metathesis reactions. Nature |
Lam JK, Zhu C, Bukhryakov KV, et al. (2016) Synthesis and Evaluation of Molybdenum and Tungsten Monoaryloxide Halide Alkylidene Complexes for Z-Selective Cross-Metathesis of Cyclooctene and Z-1,2-Dichloroethylene. Journal of the American Chemical Society. 138: 15774-15783 |
Lam JK, Joseph SB, Vanderwal CD. (2014) A Zincke aldehyde approach to gelsemine Tetrahedron Letters. 56: 3165-3168 |
Lam JK, Pham HV, Houk KN, et al. (2013) Computation and experiment reveal that the ring-rearrangement metathesis of Himbert cycloadducts can be subject to kinetic or thermodynamic control. Journal of the American Chemical Society. 135: 17585-94 |
Schmidt Y, Lam JK, Pham HV, et al. (2013) Studies on the Himbert intramolecular arene/allene Diels-Alder cycloaddition. Mechanistic studies and expansion of scope to all-carbon tethers. Journal of the American Chemical Society. 135: 7339-48 |
Lam JK, Schmidt Y, Vanderwal CD. (2012) Complex polycyclic scaffolds by metathesis rearrangement of Himbert arene/allene cycloadducts. Organic Letters. 14: 5566-9 |
Shi BF, Zhang YH, Lam JK, et al. (2010) Pd(II)-catalyzed enantioselective C-H olefination of diphenylacetic acids. Journal of the American Chemical Society. 132: 460-1 |
Giri R, Lam JK, Yu JQ. (2010) Synthetic applications of Pd(II)-catalyzed C-H carboxylation and mechanistic insights: expedient routes to anthranilic acids, oxazolinones, and quinazolinones. Journal of the American Chemical Society. 132: 686-93 |