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Chemistry (Weinheim an Der Bergstrasse, Germany)|May 3, 2025
Strategy-Level Prodrug SynthesisPaul J Geaneotes, Paul E FloreancigAngewandte Chemie (International Ed. in English)|July 10, 2024
Potent and Selective Oxidatively Labile Ether-Based Prodrugs through Late-Stage Boronate IncorporationPaul J Geaneotes, Chasity P Janosko, Cephas Afeke, et al.Organic Letters|March 17, 2012
Synthesis of sulfur-containing heterocycles through oxidative carbon-hydrogen bond functionalizationYubo Cui, Paul E FloreancigOrganic Letters|July 22, 2015
Convergent One-Pot Oxidative [n + 1] Approaches to Spiroacetal SynthesisGuangRong Peh, Paul E FloreancigOrganic Letters|February 19, 2008
One-pot synthesis of bicyclic beta-alkoxy amides from cyanohydrin ethersQing Xiao, Paul E FloreancigOrganic Letters|June 26, 2009
Cyclization reactions through DDQ-mediated vinyl oxazolidinone oxidationLei Liu, Paul E FloreancigOrganic Letters|July 13, 2012
Synthesis of bridged inside-outside bicyclic ethers through oxidative transannular cyclization reactionsXun Han, Paul E FloreancigCurrent Opinion in Drug Discovery & Development|November 10, 2010
Stereoselective heterocycle synthesis through oxidative carbon-hydrogen bond activationLei Liu, Paul E FloreancigOrganic Letters|May 18, 2007
Intramolecular electron transfer initiated cation and radical formation through carbon-carbon bond activationWangyang Tu, Paul E FloreancigOrganic Letters|November 5, 2004
Investigations of the scope and mechanism of the tandem hydroesterification/lactonization reactionLijun Wang, Paul E FloreancigPageof 7