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Dobson

Chatfield C and A J Collins 1980. Introduction to Multivariate Analysis. London, Chapman Hall. Dobson C M, A Sali and M Karplus 1998. Protein Folding A Perspective from Theory and Experiment. [Pg.574]

Electronic Density Eunctional Theory Recent Progress and New Directions J. F. Dobson, G. Vignale, M. P. Das, Eds., Plenum, New York (1998). [Pg.46]

Terminal alkynes are only reduced in the presence of proton donors, e.g. ammonium sulfate, because the acetylide anion does not take up further electrons. If, however, an internal C—C triple bond is to be hydrogenated without any reduction of terminal, it is advisable to add sodium amide to the alkyne solution Hrst. On catalytic hydrogenation the less hindered triple bonds are reduced first (N.A. Dobson, 1955, 1961). [Pg.100]

H. F. H. Dobson, "Principal Ions and Dissolved Oxygen in Lake Ontario," in Proceedings of the 10th Conference on Great Takes Research, Toronto,... [Pg.205]

C Redfield, J Boyd, LJ Smith, RAG Smith, CM Dobson. Biochemistry 31 10431-10437, 1992. [Pg.274]

MI Sutcliffe, CM Dobson, RE Oswald. Solution structure of neuronal bungarotoxm determined by two-dimensional NMR spectroscopy Calculation of tertiary structure using systematic homologous model building, dynamical simulated annealing, and restrained molecular dynamics. Biochemistry 31 2962-2970, 1992. [Pg.305]

CM Dobson, A Sail, M Karplus. Protein folding A perspective from theory and experiment. Angew Chem Int Ed 37 868-893, 1998. [Pg.308]

Miranker, A., Dobson, C.M. Collapse and cooperativity in protein folding. Curr. Opin. Struct. Biol. [Pg.119]

The following, in alphabetical order, have reviewed one or more chapters, correcting our errors of fact or interpretation and helping to ensure they have the appropriate balance and emphasis Tom Alber (University of California, Berkeley), Tom Blundell (Cambridge University, UK), Stephen Burley (Rockefeller University), Charles Craik (University of California, San Francisco), Ken Dill (University of California, San Francisco), Chris Dobson (Oxford University, UK), Anthony Fink (Unversity of California, Santa Cruz), Robert Fletterick (University of California, San Francisco), Richard Henderson (LMB, Cambridge, UK), Werner Kiihlbrandt (MPI, Frankfurt), David Parry (Massey University, New Zealand), Greg Petsko (Brandeis University), and David Trentham (NIMR, London, UK). [Pg.424]

M. G. Lagally. In Reflection High-Energy Electron Diffraction andRflection Electron Imaging ofSutfzces. (P. K. Larsen and P. J. Dobson, Eds.) Plenum, New York, 1989. [Pg.263]

Dobson, P.J. (2000) Book review Nanotechnology opportunities missed, Contemp. Phys. 41, 159. [Pg.419]

Papaveraldine (Xanthaline), C2oHij05N. This substance forms colourless scales, m.p. 210°, yields well-crystallised yellow salts, which are dissociated in water, and reacts as a tertiary base, forming a methiodide, m.p. 133-5°. It gives an oxime existing in two stereoisomeric forms, and contains foru methoxyl groups. The demethylated product, papaveraldoline, Ci0H,ON(OH)4, has been prepared by Oberlin. Miss Dobson and W. H. Perkin have shown that the alkaloid, Xanthaline, isolated from opium by T. and H. Smith, is identical with papaveraldine. On reduetion with... [Pg.182]


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