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Natural Product Reports|July 22, 2014
The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesisMikail E Abbasov, Daniel RomoThe Journal of Organic Chemistry|December 9, 2017
Multicomponent, Enantioselective Michael-Michael-Aldol-β-Lactonizations Delivering Complex β-LactonesKhoi N Van, Daniel RomoNatural Product Reports|October 26, 2020
Bridging the gap between natural product synthesis and drug discoveryNathanyal J Truax, Daniel RomoOrganic Letters|August 13, 2008
Facile synthesis of the trans-fused azabicyclo[3.3.0]octane core of the palau'amines and the tricyclic core of the axinellamines from a common intermediateManuel A Zancanella, Daniel RomoJournal of the American Chemical Society|June 6, 2003
Enantioselective total synthesis of (+)-dibromophakellstatinKarine G Poullennec, Daniel RomoThe Journal of Organic Chemistry|November 2, 2007
Diastereoselective synthesis of tetrahydrofurans via mead reductive cyclization of keto-beta-lactones derived from the tandem Mukaiyama aldol lactonization (TMAL) processT Andrew Mitchell, Daniel RomoThe Journal of Organic Chemistry|May 22, 2013
Concise synthesis of the isothiourea organocatalysts homobenzotetramisole and derivativesBeatrice Ranieri, Omar Robles, Daniel RomoTetrahedron Letters|February 13, 2023
Total Synthesis of (±)-N-Methyldibromoisophakellin and N-Methylugibohlin via Net [3+2] Cycloguanidinylations Employing 2-Amido-1,3-Diamino-Allyl CationsNobuyuki Matsumoto, Taehwan Hwang, Daniel RomoOrganic Letters|May 5, 2007
Concise total synthesis of (+/-)-salinosporamide A, (+/-)-cinnabaramide A, and derivatives via a bis-cyclization process: implications for a biosynthetic pathway?Gil Ma, Henry Nguyen, Daniel RomoOrganic Letters|November 5, 2005
Studies toward a marine toxin immunogen: enantioselective synthesis of the spirocyclic imine of (-)-gymnodimineKe Kong, Ziad Moussa, Daniel RomoPageof 699