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- Unusual LCST-type behaviour found in binary mixtures of choline-based ionic liquids with ethers. Anabela J. L. Costa, Mário R. C. Soromenho, Karina Shimizu, José M. S. S. Esperança, José N. Canongia Lopes, Luís Paulo N. Rebelo
, RSC Adv.
, 2013
, 3
, 10262
- Reactions of methylene with ethers. Part 1.—Dimethyl ether, methyl ethyl ether, methyl n-propyl ether, methyl-isopropyl ether, methyl-t-butyl ether and tetrahydrofuran. H. M. Frey, M. A. Voisey
, Trans. Faraday Soc.
, 1968
, 64
, 954
- Use of a neural network to determine the normal boiling points of acyclic ethers, peroxides, acetals and their sulfur analogues. Driss Cherqaoui, Didier Villemin, Abdelhalim Mesbah, Jean-Michel Cense, Vladimir Kvasnicka
, J. Chem. Soc., Faraday Trans.
, 1994
, 90
, 2015
- CXI.—The systems n-butyl alcohol–water and n-butyl alcohol–acetone–water. David Charles Jones
, J. Chem. Soc.
, 1929
, 799
- Alkyl–oxygen heterolysis in carboxylic esters and related compounds. A. G. Davies, J. Kenyon
, Q. Rev. Chem. Soc.
, 1955
, 9
, 203
- 115. The reaction of 1 : 4-dichloro-2 : 3-epoxybutane with sodium methoxide. A. W. Adams, E. G. E. Hawkins, G. F. Oldham, R. D. Thompson
, J. Chem. Soc.
, 1959
, 559
- Electrocatalytic synthesis: an environmentally benign alternative for radical-mediated aryl/alkenyl C(sp2)–C(sp3) cross-coupling reactions. Mu-Jia Luo, Haixin Ding, Ruchun Yang, Qiang Xiao
, Green Chem.
, 2022
, 24
, 9373
- Experimental verification of the intermediacy and interconversion of ion–neutral complexes as radical cations dissociate. Steen Hammerum, Henri Edouard Audier
, J. Chem. Soc., Chem. Commun.
, 1988
, 860
- Studies on the Lewis acid mediated cleavage of α-aminoacetals: synthesis of novel 1,2-aminoethers, and evidence for α-alkoxy aziridinium ion intermediates. Mark A. Graham, Alan H. Wadsworth, Abdul Zahid, Christopher M. Rayner
, Org. Biomol. Chem.
, 2003
, 1
, 834
- 306. Co-catalysis in Friedel–Crafts reactions. Part V. The isomerisation of butenes by boron fluoride–acetic acid. Joan M. Clayton, A. M. Eastham
, J. Chem. Soc.
, 1963
, 1636