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Organic & Biomolecular Chemistry|December 14, 2011
Lewis acid promoted intramolecular (3 + 2) 'cycloadditions' of methyleneaziridines with alkene and alkyne acceptorsKaren Griffin, Cyril Montagne, Cam Thuy Hoang, et al.
Chemical Communications (Cambridge, England)|November 16, 2004
Biosynthetic studies on the azinomycins: the pathway to the naphthoate fragmentChristophe Corre, Cyrille A S Landreau, Michael Shipman, et al.
Organic & Biomolecular Chemistry|March 24, 2005
On the origin of the DNA sequence selectivity of the azinomycinsRachel C LePla, Cyrille A S Landreau, Michael Shipman, et al.
The Journal of Organic Chemistry|June 22, 2021
Synthesis of Arylidene-β-lactams via exo-Selective Matsuda-Heck Arylation of Methylene-β-lactamsNastja Riemer, Martin Riemer, Mandy Krüger, et al.
The Journal of Organic Chemistry|November 30, 2017
Synthesis of 4,5-Diazaspiro[2.3]hexanes and 1,2-Diazaspiro[3.3]heptanes as Hexahydropyridazine AnaloguesAlpa K Pancholi, Greg P Iacobini, Guy J Clarkson, et al.
Chemical Communications (Cambridge, England)|June 19, 2013
Photochemical control of molecular motion associated with pyramidal inversionAlexander J Hough, Ivan Prokes, James H R Tucker, et al.
Organic & Biomolecular Chemistry|September 2, 2003
Preparation and reactivity of imino glycals: stereocontrolled, divergent approach to imino sugarsPaul J Dransfield, Paul M Gore, Ivan Prokes, et al.
Organic Letters|June 7, 2017
Solid-Phase Synthesis of Oxetane Modified PeptidesJonathan D Beadle, Astrid Knuhtsen, Alex Hoose, et al.
Organic & Biomolecular Chemistry|September 19, 2014
Stereocontrolled lithiation/trapping of chiral 2-alkylideneaziridines: investigation into the role of the aziridine nitrogen stereodynamicsRosmara Mansueto, Leonardo Degennaro, Jean-François Brière, et al.
Chemical Communications (Cambridge, England)|December 1, 2007
Umbrella motion in aziridines: use of simple chemical inputs to reversibly control the rate of pyramidal inversionMark W Davies, Adam J Clarke, Guy J Clarkson, et al.
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