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Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides.
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Cycloaddition of cyclobutenone and azomethine imine enabled by chiral isothiourea organic catalysts.
Chem Sci. 2015 Oct 1;6(10):6008-6012. doi: 10.1039/c5sc01972a. Epub 2015 Jul 20.
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1,3-Dipolar cycloadditions of azomethine imines.
Org Biomol Chem. 2015 Aug 28;13(32):8596-636. doi: 10.1039/c5ob01086a. Epub 2015 Jul 3.
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N-Heterocyclic carbene-catalyzed [2+3] cyclocondensation of α-chloroaldehydes with azomethine imines.
Chem Commun (Camb). 2015 Jun 7;51(45):9328-31. doi: 10.1039/c5cc01238d.
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Understanding bond formation in polar one-step reactions. Topological analyses of the reaction between nitrones and lithium ynolates.
J Org Chem. 2015 Apr 17;80(8):4076-83. doi: 10.1021/acs.joc.5b00413. Epub 2015 Apr 1.
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Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals.
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Enantioselective 1,3-dipolar cycloaddition of azomethine imines with propioloylpyrazoles induced by chiral π-cation catalysts.
J Am Chem Soc. 2014 Sep 24;136(38):13198-201. doi: 10.1021/ja508441t. Epub 2014 Sep 16.
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Fluxionally chiral DMAP catalysts: kinetic resolution of axially chiral biaryl compounds.
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Development of a tailor-made bis(oxazolidine)pyridine-metal catalyst for the [3+2] cycloaddition of azomethine imines with propiolates.
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Catalytic asymmetric three-component 1,3-dipolar cycloaddition of aldehydes, hydrazides, and alkynes.
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