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Synthesis of organic compounds

The silver fluorocomplexes, ie, silver hexafluoroantimonate [26042-64-8], AgSbF silver hexafluorophosphate [26042-63-7], AgPF silver tetrafluoroborate [14104-20-2], AgBF and other salts such as silver trifluoromethane sulfonate [2923-28-6], CF SO Ag, and silver trifluoroacetate [2966-50-9], CF COOAg, play an important role in the synthesis of organic compounds and have gained potential industrial importance. [Pg.235]

Methods for Synthesis of Organic Compounds Mth Nitrogen-Fluorine Bonding (Russ) Fokin A V Studnev, Y N, Kuznetsova, L G Reakt< Metndy h< led Org Soedm 24 7 66 819... [Pg.13]

M. Y. Fioshin u. A. P. Tomilov, Electrochemical Dimerisation - a promising Method for the Synthesis of organic Compounds, Khim. Prom. 1964. 649. [Pg.785]

The Diels-Alder reaction, in which two alkenes combine to give a new product, is one of the most frequently used reactions for the synthesis of organic compounds. Thousands of examples are found in the chemical literature. The reaction of butadiene is a simple example. [Pg.1072]

As already mentioned in the introduction, various fundamental and many empirical results have been published. Although photoelectrochemical cells are easily made, many problems concerning the stability of semiconductors and the function of catalysts still remain to be solved. There are few other approaches such as for instance sensitization (see e.g.) which are not treated here. In addition it should be mentioned that photoelectrochemical systems have been used for light induced synthesis of organic compounds (see e.g.) which could also not be considered in this article. [Pg.109]

Chou Y-L, Morrissey MM, Mohan R. Novel serine-based linker for the solid-phase synthesis of organic compounds. Tetrahedron Lett 1998 39 757-760. [Pg.223]

The single-bond compounds between Si, Ge, and Sn and chalcogens (S, Se, Te) are reactive and used as synthetic intermediates in the synthesis of organic compounds, organochalcogen compounds, organo-silicon, -germanium and -tin compounds, and transition metal-chalcogen complexes and clusters. [Pg.195]

Miller S. L. (2000). The Endogenous Synthesis of Organic Compounds in The Molecular Origins of Life, Editor BrackA. CUP (2000). [Pg.332]

The traditional way of producing derivatives for analytical purposes aims at preserving, as much as possible, the important structural features of the analyte. In the case of organotin compounds this means that the tin moieties of the compound should appear in the derivative, as occurs in the methods described in Section V.A. Nevertheless, many organotin compounds are important intermediates in the synthesis of organic compounds devoid of metallic atoms. Such procedures can afford good derivatizing schemes, as described in Section V.B. [Pg.403]

A. P. Tomilov, M. Ya. Fioshin and V. A. Smirnov, Electrochemical Synthesis of Organic Compounds, Chimia, Moscow, (1976). [Pg.718]

Brunner, H., Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts in Substoichiometric Quantities, 18, 129. [Pg.595]

Designed synthesis of organic compounds whether in the pharmaceutical, macromolecular, biological or pure chemical field is an art as well as a science. Of all branches of chemistry, synthesis is today the most vibrant with new techniques and methodologies and is most rapidly developing. The techniques used a decade ago have become outmoded today. [Pg.195]

Cyclopropane, C3H6, is used in the synthesis of organic compounds and as a fast-acting anesthetic. It undergoes rearrangement to form propene. If cyclopropane disappears at a rate of 0.25 mol/s, at what rate is propene being produced ... [Pg.272]

Auxiliary physical techniques in the synthesis of organic compounds... [Pg.74]

Schaeffer s salt orgchem HOC oS03Na A light-yellow to pink, water-soluble powder the sodium salt formed from 2-naphthol-6-sulfonic acid used as an intermediate in synthesis of organic compounds. sha-forz, s6lt ... [Pg.334]

Free radicals are highly reactive species and react with the CH3CI and CH3CH3 products to produce more free radicals, which, in turn, form even more products. And so it goes on until you end up with a reaction mixture containing lots of different compounds. Each of these compounds will be produced in low yields and will be difficult to isolate. It is for these reasons that reactions involving homolytic fission are unsuitable in the synthesis of organic compounds. [Pg.55]


See other pages where Synthesis of organic compounds is mentioned: [Pg.9]    [Pg.236]    [Pg.115]    [Pg.62]    [Pg.136]    [Pg.664]    [Pg.155]    [Pg.30]    [Pg.31]    [Pg.1622]    [Pg.13]    [Pg.158]    [Pg.568]    [Pg.1]    [Pg.113]    [Pg.252]    [Pg.109]    [Pg.136]    [Pg.39]    [Pg.86]    [Pg.148]    [Pg.461]    [Pg.43]    [Pg.242]    [Pg.92]    [Pg.276]    [Pg.379]    [Pg.27]    [Pg.97]    [Pg.185]    [Pg.209]    [Pg.240]    [Pg.267]   
See also in sourсe #XX -- [ Pg.68 ]

See also in sourсe #XX -- [ Pg.475 ]

See also in sourсe #XX -- [ Pg.1314 , Pg.1315 ]




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