Michael J. Ardolino, Ph.D.
Affiliations: | Chemistry | Boston College, Newton, MA, United States |
Area:
organic synthesis, methodologyGoogle:
"Michael Ardolino"Mean distance: 8.36 | S | N | B | C | P |
Parents
Sign in to add mentorRichard D. Broene | research assistant | Bowdoin College | ||
James P. Morken | grad student | 2014 | Boston College | |
(Synthesis of enantioenriched 1,5-dienes and 1,5-enynes by a palladium-catalyzed 3,3--reductive elimination: Methodology development and mechanistic studies.) |
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Publications
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Wright BA, Ardolino MJ. (2018) Surprising Reactivity in NiXantphos/Palladium-Catalyzed α-Arylation of Substituted Cyclopropyl Nitriles. The Journal of Organic Chemistry |
Ardolino MJ, Morken JP. (2015) Branched/linear selectivity in palladium-catalyzed allyl-allyl cross-couplings: The role of ligands. Tetrahedron. 71: 6409-6413 |
Ardolino MJ, Morken JP. (2015) Branched/linear selectivity in palladium-catalyzed allyl-allyl cross-couplings: The role of ligands Tetrahedron |
Ardolino MJ, Morken JP. (2014) Congested C-C bonds by Pd-catalyzed enantioselective allyl-allyl cross-coupling, a mechanism-guided solution. Journal of the American Chemical Society. 136: 7092-100 |
Ardolino MJ, Morken JP. (2014) ChemInform Abstract: Congested C-C Bonds by Pd-Catalyzed Enantioselective Allyl-Allyl Cross-Coupling, a Mechanism-Guided Solution. Cheminform. 45: no-no |
Ardolino MJ, Eno MS, Morken JP. (2013) Stereocontrol in Palladium-Catalyzed Propargylic Substitutions: Kinetic Resolution to give Enantioenriched 1,5-Enynes and Propargyl Acetates. Advanced Synthesis & Catalysis. 355: 3413-3419 |
Ardolino MJ, Morken JP. (2012) Construction of 1,5-enynes by stereospecific Pd-catalyzed allyl-propargyl cross-couplings. Journal of the American Chemical Society. 134: 8770-3 |
Brozek LA, Ardolino MJ, Morken JP. (2011) Diastereocontrol in asymmetric allyl-allyl cross-coupling: stereocontrolled reaction of prochiral allylboronates with prochiral allyl chlorides. Journal of the American Chemical Society. 133: 16778-81 |