Publications
Found 11 results
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Filters: Author is Martin Kotora and First Letter Of Title is E [Clear All Filters]
An easy route to atropoisomeric bipyridine N,N′-dioxides and allylation of aldehydes. Tetrahedron: Asymmetry 2006, 17 (22), 3185-3191 DOI: 10.1016/j.tetasy.2006.11.025.
Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.
Enantioselective Allylation of Aldehydes Catalyzed by Diastereoisomeric Bis(tetrahydroisoquinoline) N,N′-Dioxides. European Journal of Organic Chemistry 2010, 2010 (36), 7040-7044 DOI: 10.1002/ejoc.201001219.
Enantioselective epoxide ring opening catalyzed by bis(tetrahydroisoquinoline) N,N′-dioxides. Collection of Czechoslovak Chemical Communications 2011, 76 (5), 415-422 DOI: 10.1135/cccc2011024.
Enantioselective Synthesis of (-)-Methoxyestrone. European Journal of Organic Chemistry 2011, 2011 (18), 3279-3282 DOI: 10.1002/ejoc.201100317.
Enantioselective Allylation of Selected ortho-Substituted Benzaldehydes: A Comparative Study. European Journal of Organic Chemistry 2014, 2014 (32), 7245-7252 DOI: 10.1002/ejoc.201403034.
Enantioselective Allylation of tert-Butyldimethylsilyl-Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana. European Journal of Organic Chemistry 2014, 2014 (34), 7556-7560 DOI: 10.1002/ejoc.201403094.
Enantioselective Allylation of Thiophene-2-carbaldehyde: Formal Total Synthesis of Duloxetine. Advanced Synthesis & Catalysis 2014, 356 (1), 199-204 DOI: 10.1002/adsc.201300849.
Enantioselective Allylation of (2E,4E)-2,4-Dimethylhexadienal: Synthesis of (5R,6S)-(+)-Pteroenone. Chemistry - A European Journal 2015, 21 (20), 7408-7412 DOI: 10.1002/chem.201500050.
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.