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Recent Contributions from the Leighton Group


66

"A Tandem Cross-Metathesis/Semipinacol Rearrangement Reaction" Plummer, C. W.; Soheili, A.; Leighton, J. L. Org. Lett. 2012, 14, ASAP. [Link]


65

"Direct and Highly Enantioselective Iso-Pictet–Spengler Reactions with α-Ketoamides: Access to Underexplored Indole Core Structures" Schönherr, H.; Leighton, J. L. Org. Lett. 2012, 14, ASAP. [Link]


64

"A New Synthesis of Pyrrolidines by Way of an Enantioselective Mannich/Diastereoselective Hydroamination Reaction Sequence" Baxter Vu, J. M.; Leighton, J. L. Org. Lett. 2011, 13, 4056-4059. [Link]


63

"Toward More "Ideal" Polyketide Natural Product Synthesis: A Step-Economical Synthesis of Zincophorin Methyl Ester" Harrison, T. J.; Ho, S.; Leighton, J. L. J. Am. Chem. Soc. 2011, 133, 7308-7311. [Link]


62

"A More Comprehensive and Highly Practical Solution to Enantioselective Aldehyde Crotylation" Kim, H.; Ho, S.; Leighton, J. L. J. Am. Chem. Soc. 2011, 133, 6517-6520. [Link]


61

"Highly Enantioselective Mannich Reactions with α-Aryl Silyl Ketene Acetals and Imines" Notte, G. T.; Baxter Vu, J. M.; Leighton, J. L. Org. Lett 2011, 13, 816-818. [Link]


60

"Enantioselective (Formal) Aza-Diels−Alder Reactions with Non-Danishefsky-Type Dienes" Tambar, U. K.; Lee, S. K.; Leighton, J. L. J. Am. Chem. Soc. 2010, 132, 10248–10250. [Link]


59

"Highly enantioselective formal aza-Diels–Alder reactions with acylhydrazones and Danishefsky's diene promoted by a silicon Lewis acid" Lee, S. K.; Tambar, U. K.; Perl, N. R.; Leighton, J. L. Tetrahedron 2010, 66, 4769-4774. [Link]

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Email: leighton@chem.columbia.edu



Maintained by Paul Tanis | Last Updated: 30 April 2012