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Organic Letters|July 6, 2010
Exploiting the chemistry of strained rings: synthesis of indoles via domino reaction of aryl iodides with 2H-azirinesDavid A Candito, Mark LautensJournal of the American Chemical Society|August 22, 2012
Development of an intramolecular aryne ene reaction and application to the formal synthesis of (±)-crinineDavid A Candito, Dennis Dobrovolsky, Mark LautensJournal of the American Chemical Society|August 23, 2011
Intramolecular aryne-ene reaction: synthetic and mechanistic studiesDavid A Candito, Jane Panteleev, Mark LautensOrganic Letters|October 19, 2010
Palladium-catalyzed reductive ortho-arylation: evidence for the decomposition of 1,2-dimethoxyethane and subsequent arylpalladium(II) reductionAndrew Martins, David A Candito, Mark LautensNatural Product Reports|March 3, 2015
Lessons from the synthetic chemist natureGerrit Jürjens, Andreas Kirschning, David A CanditoOrganic Letters|February 26, 2011
Formal synthesis of nitidine and NK109 via palladium-catalyzed domino direct arylation/N-arylation of aryl triflatesMathieu Blanchot, David A Candito, Florent Larnaud, et al.Angewandte Chemie (International Ed. in English)|January 29, 2009
Exploiting the divergent reactivity of aryl-palladium intermediates for the rapid assembly of fluorene and phenanthrene derivativesYa-Bin Zhao, Brian Mariampillai, David A Candito, et al.The Journal of Organic Chemistry|March 23, 2021
Development of a Flexible and Robust Synthesis of Tetrahydrofuro[3,4-b]furan Nucleoside AnaloguesDavid A Candito, Yingchun Ye, Ryan V Quiroz, et al.ACS Medicinal Chemistry Letters|April 16, 2021
Discovery of Diaminopyrimidine Carboxamide HPK1 Inhibitors as Preclinical Immunotherapy Tool CompoundsBrandon A Vara, Samuel M Levi, Abdelghani Achab, et al.Journal of Medicinal Chemistry|December 8, 2022
Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1H-Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson's DiseaseDavid A Candito, Vladimir Simov, Anmol Gulati, et al.Pageof 2