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Beilstein Journal of Organic Chemistry|July 25, 2020
Facile synthesis of 7-alkyl-1,2,3,4-tetrahydro-1,8-naphthyridines as arginine mimetics using a Horner-Wadsworth-Emmons-based approachRhys A Lippa, John A Murphy, Tim N Barrett
Organic & Biomolecular Chemistry|April 1, 2017
A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene-arene couplingFlorimond Cumine, Shengze Zhou, Tell Tuttle, et al.
Beilstein Journal of Organic Chemistry|January 1, 2015
One-pot functionalisation of N-substituted tetrahydroisoquinolines by photooxidation and tunable organometallic trapping of iminium intermediatesJoshua P Barham, Matthew P John, John A Murphy
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 21, 2025
A Convergent Radical Cascade for the Synthesis of AzaindanesChelsea D Grace, John A Murphy, Simon M Nicolle
Organic Letters|August 2, 2003
Synthesis of muscothiazoles A and B: Critical role of methyl group substitution in RCM-based syntheses of macrocyclesAurélien G J Commeureuc, John A Murphy, Mark L Dewis
Case Reports in Gastroenterology|April 15, 2011
Anterior abdominal wall abscess secondary to subcutaneous gallstonesJohn A Murphy, C Dale Vimalachandran, Nathan Howes, et al.
Beilstein Journal of Organic Chemistry|March 5, 2009
Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicalsMohan Mahesh, John A Murphy, Franck LeStrat, et al.
Molecules (Basel, Switzerland)|November 27, 2021
Radical and Ionic Mechanisms in Rearrangements of o-Tolyl Aryl Ethers and Amines Initiated by the Grubbs-Stoltz Reagent, Et3SiH/KOBuKrystian Kolodziejczak, Alexander J Stewart, Tell Tuttle, et al.
Angewandte Chemie (International Ed. in English)|June 22, 2019
Neutral Organic Super Electron Donors Made CatalyticSimon Rohrbach, Rushabh S Shah, Tell Tuttle, et al.
Organic Letters|September 26, 2003
Amination of arenes through electron-deficient reaction cascades of aryl epoxyazidesStuart Lang, Alan R Kennedy, John A Murphy, et al.
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