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Journal of the American Chemical Society|June 14, 2008
One-pot synthesis of highly functionalized pyridines via a rhodium carbenoid induced ring expansion of isoxazolesJames R Manning, Huw M L DaviesNature|January 25, 2008
Catalytic C-H functionalization by metal carbenoid and nitrenoid insertionHuw M L Davies, James R ManningJournal of the American Chemical Society|January 26, 2006
C-H activation as a strategic reaction: enantioselective synthesis of 4-substituted indolesHuw M L Davies, James R ManningTetrahedron|January 17, 2009
Efficient route to 4H-1,3-oxazines through ring expansion of isoxazoles by rhodium carbenoidsJames R Manning, Huw M L DaviesBioorganic & Medicinal Chemistry Letters|November 29, 2008
1-Naphthyl and 4-indolyl arylalkylamines as selective monoamine reuptake inhibitorsJames R Manning, Tammy Sexton, Steven R Childers, et al.The Journal of Organic Chemistry|September 19, 2019
Finding Opportunities from Surprises and Failures. Development of Rhodium-Stabilized Donor/Acceptor Carbenes and Their Application to Catalyst-Controlled C-H FunctionalizationHuw M L DaviesJournal of the American Chemical Society|July 12, 2011
Combined C-H functionalization/Cope rearrangement with vinyl ethers as a surrogate for the vinylogous Mukaiyama aldol reactionYajing Lian, Huw M L DaviesOrganic Letters|March 29, 2012
Rh2(S-biTISP)2-catalyzed asymmetric functionalization of indoles and pyrroles with vinylcarbenoidsYajing Lian, Huw M L DaviesOrganic Letters|May 21, 2004
Double C-H activation strategy for the asymmetric synthesis of C2-symmetric anilinesHuw M L Davies, Qihui JinJournal of the American Chemical Society|September 2, 2004
Highly diastereoselective and enantioselective C-H functionalization of 1,2-dihydronaphthalenes: a combined C-H activation/Cope rearrangement followed by a retro-Cope rearrangementHuw M L Davies, Qihui JinPageof 21