Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Chemistry acetylene

For general practical instructions concerning reactions in liquid ammonia one should consult "Preparative Acetylenic Chemistry", Elsevier, Amsterdam, 1971. [Pg.3]

X = Cl, 0-tetrahydropyranyl, 0-CH(CH3)OCjH5 The starting compounds can be easily synthesized by standard procedures in acetylene chemistry. [Pg.156]

L. Brandsma, "Preparative Acetylenic Chemistry", Elsevier Publishing Company, Amsterdam, London, New York, (1971). [Pg.271]

In 1971 we published "Preparative Acetylenic Chemistry", a collection of procedures for various acetylenic compounds. An important aim of this book was to make acetylenes more accessible, so that barriers for starting research in this field could be lowered. [Pg.280]

Acetylene-Based Routes. Walter Reppe, the father of modem acetylene chemistry, discovered the reaction of nickel carbonyl with acetylene and water or alcohols to give acryUc acid or esters (75,76). This discovery led to several processes which have been in commercial use. The original Reppe reaction requires a stoichiometric ratio of nickel carbonyl to acetylene. The Rohm and Haas modified or semicatalytic process provides 60—80% of the carbon monoxide from a separate carbon monoxide feed and the remainder from nickel carbonyl (77—78). The reactions for the synthesis of ethyl acrylate are... [Pg.155]

With each succeeding year in the 1950s and 1960s there was a swing away from coal and vegetable sources of raw materials towards petroleum. Today such products as terephthalic acid, styrene, benzene, formaldehyde, vinyl acetate and acrylonitrile are produced from petroleum sources. Large industrial concerns that had been built on acetylene chemistry became based on petrochemicals whilst coal tar is no longer an indispensable source of aromatics. [Pg.10]

P. J. Stang and F. Diederich, eds.. Modem Acetylene Chemistry, VCH Publishers, Weinheim, 1995. [Pg.398]

Internationally renowned authors, among them K. C. Nicolaou, H. Iwamura, R. H. Grubbs and H. Hopf, present the full potential of acetylene chemistry, from organic synthesis through materials science to bioorganic chemistry. [Pg.799]

Cut Out Reactive Intermediates which Waste Energy. This precept is illustrated by the general move away from acetylene chemistry to ethylene over the past two decades. [Pg.241]

The propargyl halide (15) can easily be made by acetylene chemistry,... [Pg.168]

Answer Oisconnoct.i ng the ester f i rst of all gives an acid (2), made by straightforward acetylene chemistry (Chapter 16) and an alcohol (3) which is available, but which could be made by simple Grignard chemistry. [Pg.192]

Slang PJ, Diederich F (1995) Modern acetylene chemistry. VCH, Weinheim... [Pg.40]

Scott LT, Cooney M) (1995) Macrocyclic homoconjugated polyacetylenes. In Stang PJ, Diederich F (eds) Modern acetylene chemistry. VCH, Weinheim, p 321... [Pg.40]

Keywords Acetylene chemistry. Cross-coupling reactions, Cyclo[n]carbons, Expanded radialenes. Molecular scaffolding. Nanostructures, Perethynylated chromophores, Poly(triacetylene), Tetraethynylethene. [Pg.43]

Brandsma L (1971) Preparative acetylenic chemistry, Elsevier, Amsterdam. The first edition contained the preparation of l-phenyl-l,3-butadiyne, but stated ...the compound proved to be very unstable, (and) can be stored at -20°C for a very limited period. This procedure has subsequently been deleted from the second edition (1988). [Pg.128]

Chem Int Ed Engl 33 869. de Meijere A, Kozhusov S, Haumann T, Boese R, Puls C, Cooney MJ, Scott LT (1995) Chemistry 1 124. Review Scott LT, Cooney MJ (1995) Pericyclynes. In Diederich F, Stang PJ (eds) Modern Acetylene Chemistry. Verlag Chemie, New York... [Pg.160]

Brandsma, L., in Preparative Acetylenic Chemistry, Heus-Kloos, Y. A., Van Der Heiden, R., Verkruijsse, H. D., eds., 2nd ed. Elsevier, New York, 1988 Brandsma, L., Vasilevsky, S. F., Verkruijsse, H. D., Application of Transition Metal Catalysts in Organic Synthesis. Springer-Verlag New York, 1999. [Pg.140]

Chien, J, C. W., Poly acetylene Chemistry, Physics and Materials Science, Academic Press, New York, 1984. [Pg.354]

Epoxides figure in yet other routes,58,59 while even the simple dehydration of ketonic glycols is still valuable.60 Epoxides and glycols also figure in routes based upon acetylene chemistry, to which we now proceed. [Pg.177]

In the context of modern acetylene chemistry , which serves a variety of implementations, for example new materials, special polymers, nanostructures, and supramolecular... [Pg.358]


See other pages where Chemistry acetylene is mentioned: [Pg.373]    [Pg.89]    [Pg.327]    [Pg.68]    [Pg.799]    [Pg.508]    [Pg.803]    [Pg.66]    [Pg.44]    [Pg.74]    [Pg.74]    [Pg.74]    [Pg.76]    [Pg.76]    [Pg.76]    [Pg.128]    [Pg.159]    [Pg.234]    [Pg.274]    [Pg.37]    [Pg.1928]    [Pg.251]    [Pg.976]   
See also in sourсe #XX -- [ Pg.35 ]

See also in sourсe #XX -- [ Pg.213 ]

See also in sourсe #XX -- [ Pg.281 ]

See also in sourсe #XX -- [ Pg.167 ]




SEARCH



Acetylene cycloaddition chemistry

Computational aspects, acetylene chemistry

History acetylene chemistry

Modern acetylene chemistry

Theoretical aspects, acetylene chemistry

© 2024 chempedia.info