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389Andrew M. Spring, Chin-Yang Yu, Masaki Horie and Michael L. Turner.
MEH-PPV by microwave assisted ring-opening metathesis polymerisation, Chem. Commun., 2009, 2676. Stefanie Wolf and Herbert Plenio.
On the ethenolysis of natural rubber and squalene, Green Chem., 2011, 13, 2008. José Carlos Netto-Ferreira, Monica T. Silva and Alyne M. Cardoso da Silva.
Photochemistry of cyclic vicinal tricarbonyl compounds. Laser flash photolysis study of the reaction of indane-1,2,3-trione and its 5-methoxy derivative with olefins, Photochem. Photobiol. Sci., 2002, 1, 278. G. Thiault, R. Thévenet, A. Mellouki and G. Le Bras.
OH and O-initiated oxidation of ethyl vinyl ether, Phys. Chem. Chem. Phys., 2002, 4, 613. Thomas Pauloehrl, Guillaume Delaittre, Martin Bastmeyer and Christopher Barner-Kowollik.
Ambient temperature polymer modification by in situ phototriggered deprotection and thiol–ene chemistry, Polym. Chem., 2012, 3, 1740. Eduardo C. Meurer, Hao Chen, Leah Riter, Ismael Cotte-Rodriguez, Marcos N. Eberlin and R. Graham Cooks.
Gas-phase reactions for selective detection of the explosives TNT and RDX, Chem. Commun., 2004, 0, 40. Colin M. Hayman, David S. Larsen, Jim Simpson, Karl B. Bailey and Gurmit Singh Gill.
A stereoselective synthesis of 6,6,6-trifluoro-l-daunosamine and 6,6,6-trifluoro-l-acosamine, Org. Biomol. Chem., 2006, 4, 2794. Ian W. Ashworth, David J. NelsonCurrent address: EaStCHEM, School of Chemistry, University of St. Andrews, North Haugh, St. Andrews, Fife, KY16 9ST, UK. E-mail: djn5@st-andrews.ac.uk and Jonathan M. P
ercy.
Solvent effects on Grubbs’ pre-catalyst initiation rates, Dalton Trans., 2013, 42, 4110. Ali Alaaeddine, Guillaume Couture and Bruno Ameduri.
An efficient method to synthesize vinyl ethers (VEs) that bear various halogenated or functional groups and their radical copolymerization with chlorotrifluoroethylene (CTFE) to yield functional poly(
VE-alt-CTFE) alternated copolymers, Polym. Chem., 2013, 4, 4335. Hammer Niels, Leth Lars A., Stiller Julian, Jensen Magnus E., Jørgensen Karl Anker.
Oxadendralenes in asymmetric organocatalysis for the construction of tetrahydroisochromenes, Chem. Sci., 2016