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Glaser

Created by Rainer Glaser (University of Missouri) the animations are basic mechanisms that can be presented at full screen size m your classroom The animations on the CD can be played directly from the CD or can be im ported easily into your own lecture presentation... [Pg.1333]

P. E. Glaser, Solar-Power Satellites The Emerging Energy Option, Ellis Howard, New York, 1993. [Pg.349]

Glaser and Thodos [Am. Jn.st. Chem. Eng. J., 4, 63 (1958)] give a correlation involving individual particle shape and bed porosity. Kunii and Suzuki [Jnt. ]. Heat Mass Tran.sfer, 10, 845 (1967)] discuss heat and mass transfer in packed beds of fine particles. [Pg.1059]

GLASER - CHODKIEWCZ Acetylene Coupling Polyacetylenes from monoacetylenes in the presence of copper salts. [Pg.147]

Towler, D. A., Gordon, J. L, Adams, S. R, and Glaser, L., 1988. The biology and enzymology of eukaryodc protein acylation. Annual Review of Biochemistry 57 69—99. [Pg.295]

The Glaser reaction is an oxidative coupling of terminal alkynes 1 to yield a symmetrical Z -acetylene 2 the coupling step is catalyzed by a copper salt. Closely related is the Eglinton reaction, which differs from the Glaser reaction mainly by the use of stoichiometric amounts of copper salt as oxidizing agent. [Pg.135]

Acetylene and terminal alkynes are CH-acidic compounds the proton at the carbon-carbon triple bond can be abstracted by a suitable base. Such a deprotonation is the initial step of the Glaser reaction as well as the Eglinton... [Pg.135]

The Glaser coupling reaction is carried out in aqueous ammonia or an alcohol/ammonia solution in the presence of catalytic amounts of a copper-I salt. The required copper-II species for reaction with the acetylide anion R-C=C are generated by reaction with an oxidant—usually molecular oxygen. For the Eglinton procedure, equimolar amounts of a copper-II salt are used in the presence of pyridine as base. [Pg.136]

All three coupling procedures are suitable to give high yields under mild reaction conditions. Many functional groups do not interfere. For the application in organic synthesis the Eglinton variant may be more convenient than the Glaser method a drawback however is the need for stoichiometric amounts of copper salt. [Pg.137]

Glaser oxidative coupling, 46, 41 Glucqfvranosyl chloride, 2 ACET AMIDO 2 DEOXY TRIACETATE,... [Pg.130]


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Coloristic Properties (by F. Glaser)

Coupling Eglinton—Glaser

Cross-coupling reactions Glaser reaction

Eglington-Glaser reaction

Eglinton-Glaser oxidative coupling

GLASER - CHODKIEWCZ Acetylene coupling

Glaser Homocoupling and the Cadiot-Chodkiewicz Heterocoupling Reaction

Glaser coupling

Glaser coupling copper

Glaser coupling homocoupling

Glaser coupling reaction

Glaser modified

Glaser oxidation

Glaser oxidative

Glaser oxidative coupling reaction

Glaser procedure

Glaser process

Glaser reaction

Glaser, Christoph

Glaser, Christophe

Glaser, Christopher

Glaser, Donald

Glaser-Hay coupling

Glaser-Hay coupling reaction

Glaser-type Couplings

Glaser-type alkyne coupling

Glaser-type reaction

Kiecolt-Glaser

Oxidative Glaser coupling

Template Glaser coupling

Watson-Glaser Critical Thinking Appraisal

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