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Fraser

Fraser, Ken (1991) Managing Drilling Operations, 246p, Elsevier... [Pg.373]

Fraser G T and Pine A S 1986 Van der Waals potentials from the infrared speotra of rare gas-HF oomplexes J. Chem. Phys. 85 2502-15... [Pg.2453]

The large sulfur atom is a preferred reaction site in synthetic intermediates to introduce chirality into a carbon compound. Thermal equilibrations of chiral sulfoxides are slow, and parbanions with lithium or sodium as counterions on a chiral carbon atom adjacent to a sulfoxide group maintain their chirality. The benzylic proton of chiral sulfoxides is removed stereoselectively by strong bases. The largest groups prefer the anti conformation, e.g. phenyl and oxygen in the first example, phenyl and rert-butyl in the second. Deprotonation occurs at the methylene group on the least hindered site adjacent to the unshared electron pair of the sulfur atom (R.R. Fraser, 1972 F. Montanari, 1975). [Pg.8]

F. W. Fraser and C. B. Belcher, "Mineralogical Studies of the Groote Eylandt Manganese Ore Deposits," Proceedings Mustralasian Institute of Minerals and Metallurgy tFo. 254, June 1975. [Pg.499]

Shortly after Simpson s successful use of chloroform in Edinburgh, Fraser began making pure anesthetic chloroform on a small scale in Nova... [Pg.523]

A straightforward calculation of A has been performed by Fraser [1989] within the framework of the one-dimensional model of concerted interconversion. The diabatic terms were taken in the form... [Pg.125]


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Fraser Stoddart (Sheffield)

Fraser Williams Scientific Systems, Ltd

Fraser competence

Fraser equations

Fraser mechanisms

Fraser, Frank

Fraser-Reid

Fraser-Reid coupling

Fraser-Reid pentenyl glycosylation

Fraser-Reid s laboratories

Fraser-Reid synthesis

Fraser-Reid, Bert

Mechanistic analysis of the Fraser-Reid ()-silphiperfolene synthesis

Melnick Fraser syndrome

Simon Fraser University

Stoddart, J. Fraser

The Fraser-Reid retrosynthetic analysis of (-)-silphiperfolene

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