当前位置: X-MOL首页全球导师 海外导师 › Geary, Laina M.

个人简介

Banting NSERC Postdoctoral Fellow (2010-2014), University of Texas at Austin (M. J. Krische) Ph.D. (2010), University of Manitoba (P. G. Hultin) B.Sc. Hons. (2005), University of Manitoba

研究领域

Research in the Geary laboratory will focus on the development and application of transition metal chemistry in catalysis and synthetic chemistry to the formation of carbon-carbon bonds. The research will be divided into three general themes. The first will focus on the catalytic generation of reactive intermediates. By avoiding stoichiometric, preformation of highly reactive intermediates, we aim to direct the reactivity of these species in a controlled and selective manner. A second area of focus will be on rendering traditional, stoichiometric organic reactions into catalytic processes. A third area of focus is the invention of new catalytic reactions for the construction of carbon-carbon bonds. These are not mutually exclusive concepts, and the interplay between two or more areas will drive the research program. The study of reaction mechanism will be central to all projects and will lead to both a deeper understanding of chemical processes and lead to the discovery of new chemistry. One key concept in the design of projects involves the availability of the starting materials. The degrees of separation between the commodity or feedstock chemical and the starting material for the C-C bond forming reaction should be kept to a minimum, and are ideally zero. This necessitates the conceptualization of targets and goals from the very beginning, and provides a focus for the idealization of chemistries developed. The terms atom economy, step economy, and redox economy frequently appear in the literature, and serve to emphasize the importance of chemoselectivity in any transformation. High chemoselectivity is a standing goal to maximize the functional group compatibility and minimize substrate preactivation. Students will get training in organic synthesis, organometallic chemistry, and asymmetric catalysis within the broad goal of simplicity to complexity via C-C bond formation.

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

Geary, L.M.; Glasspoole, B.W.; Kim, M.M.; Krische, M.J. Successive C-C Coupling of Dienes to Vicinally Dioxygenated Hydrocarbons: Ruthenium Catalyzed [4+2] Cycloaddition across the Diol, Hydroxycarbonyl or Dione Oxidation Levels. J. Am. Chem. Soc. 2013, 135, 3796-3799. Geary, L.M.; Leung, J.C.; Krische, M.J. Ruthenium Catalyzed Reductive Coupling of 1,3-Enynes and Aldehydes via Transfer Hydrogenation: anti-Diastereoselective Carbonyl Propargylation. Chem. Eur. J. 2012, 18, 16823-16827. Leung, J.C.; Geary, L.M.; Chen, T.-Y.; Zbieg, J.R.; Krische, M.J. Direct, Redox-Neutral Prenylation and Geranylation of Secondary Carbinol C–H Bonds: C4-Regioselectivity in Ruthenium-Catalyzed C–C Couplings of Dienes to alpha-Hydroxy Esters. J. Am. Chem. Soc. 2012, 134, 15700-15703. Woo, S.K.; Geary, L.M.; Krische, M.J. Enantioselective Carbonyl Propargylation by Iridium-Catalyzed Transfer Hydrogenative Coupling of Alcohols and Propargyl Chloride. Angew. Chem., Int. Ed. 2012, 51, 7830-7834. Geary, L.M.; Woo, S.K.; Leung, J.C.; Krische, M.J. Diastereo- and Enantioselective Iridium Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents. Angew. Chem., Int. Ed. 2012, 51, 2972-2976. Geary, L.M.; Hultin, P.G. A Palladium-Catalyzed Modular Assembly of Electron–Rich Alkenes, Dienes, Trienes and Enynes from (E)-1,2-Dichlorovinyl Phenyl Ether. J. Org. Chem. 2010, 75, 6354-6371. Geary, L.M.; Hultin, P.G. 2-Substituted Benzo[b]furans from (E)-1,2-Dichlorovinyl Ethers and Organoboron Reagents: Scope and Mechanistic Investigations into the One-Pot Suzuki Coupling/Direct Arylation. Eur. J. Org. Chem. 2010, 5563-5573. Geary, L.M.; Hultin, P.G. Modular Construction of 2-Substituted Benzo[b]furans from 1,2-Dichlorovinyl Ethers. Org. Lett. 2009, 11, 5478-5481. Geary, L.M.; Hultin, P.G. The State of the Art in Asymmetric Synthesis: The Aldol Reaction as a Case Study. Tetrahedron: Asymmetry 2009, 20, 131-173. Hein, J.E.; Geary, L.M.; Jaworski, A.A.; Hultin, P.G. Practical Synthesis of Fluorous Oxazolidinone Chiral Auxiliaries from α-Amino Acids. J. Org. Chem. 2005, 70, 9940-9946.

推荐链接
down
wechat
bug