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Stephens

STEPHEN,H, STEPHEN,T E0S /S0LUBIL1TIES OF INORGANIC MO ORGANIC COMPOUNDS,MACMILLAN CO, NEW YaRK(1964) ... [Pg.207]

Stephen, H., Stephen, T., "Solubilities of Inorganic and Organic Compounds," Pergamon Press, New York (1963). [Pg.210]

Stephen Gould s writing is elegant, erudite, witty, coherent and forceful - Richard Dawkins, Nature... [Pg.441]

Work expands so as to fill the time available for its completion that law underlies this extraordinarily tunny and witty book (Stephen Potter in the Sunday Times) which also makes some painfully serious points for those in business or the Civil Service. [Pg.445]

BE-1426 Structural integrity assessment procedures for European industry Mr. E. Stephen Wabiter British Steel PLC... [Pg.936]

George R Darling, Stephen Holloway and Charles Rettner... [Pg.898]

Figure Bl.26.1. Sorption isothemi for chemisorption of hydrogen on palladium film at 273 K (Stephens S J 19597. Phys. Chem.. 63 188-94). Figure Bl.26.1. Sorption isothemi for chemisorption of hydrogen on palladium film at 273 K (Stephens S J 19597. Phys. Chem.. 63 188-94).
Stephens P W, Mihaly L, Lee P L, Whetten R L, Huang S-M, Kaner R, Diederioh F and Holozer K 1991 Struoture of single phase superoonduoting K,Cgg Nature 351 632... [Pg.2428]

Stephens P W, Bortei G, Faigei G, Tegze M, Janossy A, Pekker S, Oszianyi G and Forro L 1994 Poiymerio... [Pg.2429]

Kurst G R, R A Stephens and R W Phippen 1990. Computer Simulation Studies of Anisotropic iystems XIX. Mesophases Formed by the Gay-Berne Model Mesogen. Liquid Crystals 8 451-464. e F J, F Has and M Orozco 1990. Comparative Study of the Molecular Electrostatic Potential Ibtained from Different Wavefunctions - Reliability of the Semi-Empirical MNDO Wavefunction. oumal of Computational Chemistry 11 416-430. [Pg.268]

From nitriles by treatment with anhydrous Stannous chloride dissolved in ether saturated with hydrogen chloride the resulting crystaUine aldimine stannichloride, [(RCH=NHj)2] SnCl, or (RCH=NH,HCl)2SnCl4, is hydrolysed by warm water, and the aldehyde is isolated by distillation with steam or by extraction with a solvent (Stephen reaction), for example, for R = CH3(CH2)4, i.e., n-amyl ... [Pg.318]

From nitriles by Stephen s reaction (see under Aliphatic Aldehydes and Section 111,64), for example ... [Pg.691]

Stephen reaction Stobbe condensation UUmann reaction Willgerodt reaction. ... [Pg.1211]

John von Neuman, one of the greatest mathematicians of the twentieth century, believed that the sciences, in essence, do not try to explain, they hardly even try to interpret they mainly make models. By a model he meant a mathematical construct that, with the addition of certain verbal interpretations, describes observed phenomena. The justification of such a mathematical construct is solely and precisely that it is expected to work. Stephen Hawking also believes that physical theories are just mathematical models we construct and that it is meaningless to ask whether they correspond to reality, just as it is to ask whether they predict observations. [Pg.10]

The Stephen s method allows the reduction of nitriles by stannous chloride in acid medium. If the amine chlorhydrate initially formed is hydrolyzed, the corresponding aldehyde is obtained (37, 91). Harington and Moggridge (37) have reduced 4-methyl-5-cyanothiazole by this method (Scheme 23). However, Robba and Le Guen (91) did not obtain the expected products with 4.5-dicyanothiazole and 2-methyl-4,5-dicyanothiazole. These compounds have been reduced with diisobutyl-aluminium hydride with very low yields (3 to 6%) (Scheme 24). In other conditions the reaction gives a thiazole nitrile aldehyde with the same yield as that of the dialdehyde. [Pg.531]

As mentioned previously, aldehydes can be prepared by Stephen s method of reduction of nitriles by stannous chloride (37, 91). Polaro-graphic reduction of thiazolecarboxylic acids and their derivatives gives lower yields of aldehydes (58). Ozonolysis of styrylthiazoles, for example, 2-styryl-4-methylthiazole, followed by catalytic reduction gives aldehyde with 47% yield of crude product (30). [Pg.533]


See other pages where Stephens is mentioned: [Pg.191]    [Pg.201]    [Pg.202]    [Pg.209]    [Pg.209]    [Pg.209]    [Pg.209]    [Pg.475]    [Pg.441]    [Pg.447]    [Pg.326]    [Pg.211]    [Pg.1093]    [Pg.2428]    [Pg.157]    [Pg.198]    [Pg.317]    [Pg.380]    [Pg.24]    [Pg.345]    [Pg.40]    [Pg.228]    [Pg.228]    [Pg.137]    [Pg.302]    [Pg.343]    [Pg.19]    [Pg.37]   
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See also in sourсe #XX -- [ Pg.238 ]

See also in sourсe #XX -- [ Pg.430 ]

See also in sourсe #XX -- [ Pg.44 ]

See also in sourсe #XX -- [ Pg.330 , Pg.338 ]




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Acetylide formation, Castro-Stephens reaction

Ada Hitchins (Mrs. Stephens)

Alkynylcopper Stephens-Castro reaction

Ambrose, Stephen

Angyal, Stephen ]., John

Anopheles Stephens

Ball, Stephen

Berry, R. Stephen

Boliang Lou, Hoan Khai Huynh, and Stephen Hanessian ntroduction

Breyer, Stephen

Brown, Stephen

Brunauer, Stephen

Brush, Stephen

Buckingham-Stephens theory

Burley, Stephen

Cadiot-Chodkiewicz reaction, Castro-Stephens

Castro-Stephens indole synthesis

Castro-Stephens protocol

Castro-Stephens reaction copper acetylide preparation

Castro-Stephens reaction copper-catalyzed Sonogashira

Castro-Stephens reaction formation

Castro-Stephens-Sonogashira reaction

Catenated Nitrogen Ligands Part David S. Moore and Stephen D. Robinson

Clucas, Stephen

Copper acetylide Castro-Stephens reaction

Covey, Stephen

Crane, Stephen

Crisp, Stephen

Davies, Stephen

DeVito, Stephen

Douglas, Stephen

Edited by R. Stephen Berry and Joshua Jortner. Series editor Stuart A. Rice

Emmens, Stephen

Essential Physiological Biochemistry: An organ-based approach Stephen Reed

Essential Physiological Biochemistry: An organ-based approach Stephen Reed 2009 John Wiley Sons, Ltd

Fried, Stephen

Fundamental Principles of Polymeric Materials, Third Edition. Christopher S. Brazel and Stephen L. Rosen

Gosson, Stephen

Gould, Stephen

Gould, Stephen Jay

Gray, Stephen

Greenblatt, Stephen

Halbrook, Stephen

Hales, Stephen

Hanessian, Stephen

Hanessian, Stephen, Deoxy Sugars

Harrison, Stephen

Hawking, Stephen

Hawking, Stephen, physical

Heath, Stephen

II 15 Pauson-Khand Type Reactions Stephen L. Buchwald, Frederick A. Hicks

Jackson, Stephen

Johnson, Stephen

Joseph, Stephen

Kaplan, Stephen

Kent, Stephen

King, Stephen

Ledogar, Ambassador, Stephen

Lewis, Stephen

Lincoln, Stephen

Lippard, Stephen

Lovell, Stephen

Lynch, Stephen

Mann, Stephen

Maurer, Stephen

Mayo, Stephen

McFadyen-Stephens aldehyde synthesis

Melville, Stephen

Meyer, Stephen

Mitchel, Stephen

Modified Stephen reduction

Nelson, Stephen

Newell, Stephens

Oliver, Stephen

Orgel, Stephen

Phillips, Stephen

Phosphines Castro-Stephens reaction, catalytic

Port Stephens Fisheries Institute

Pyridines Castro-Stephens reaction

Rachman, Stephen

Reynolds, Stephen

Robertson Stephens

Ross, Stephen

Royce, Stephen

STEPHEN Aldehyde synthesis

STEPHENS-CASTRO Acetylene

Scale-Up of Solid Dosage Forms Colleen E. Ruegger, Alan Royce, Matthew J. Mollan, Jr., Robert Wagner, Stephen Valazza, and Mark Mecadon

Skinner, Stephen

Smith, Stephen

Statistical Issues in Drug Development, 2nd Edition. Stephen Senn

Stephen J. Lombardo

Stephen J. de Mora 1 An Overview of Marine Pollution

Stephen M. Kelly 2 Ferroelectric Liquid Crystals

Stephen Mason

Stephen method

Stephen reaction

Stephen reduction

Stephen reduction nitriles

Stephen, Adrian

Stephen, Caroline

Stephen, Harry

Stephen, Thoby

Stephen, Vanessa

Stephens coupling

Stephens formalism

Stephens rearrangement

Stephens theory

Stephens, Donald

Stephens, Gregory

Stephens, Major

Stephens, Richard

Stephens, Samuel

Stephens-Castro coupling

Stephens-Castro coupling alkynic ketones

Stephens-Castro coupling copper acetylide intermediates

Stephens-Castro reaction

Stephens-Castro reaction, copper-catalyzed

Talty, Stephen

Teret, Stephen

The Stephens-Castro Reaction

Timoshenko, Stephen

Toulmin, Stephen

Wallace, Stephen

Weinberg, Stephen

Welford, Stephen

White, Stephen

Wilson, Stephen

Wise, Stephen

Withers, Stephen

Wolfram, Stephen

Younger, Stephen

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