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11.
Examples of sonochemical reactions occuring under heterogeneous conditions are discussed with respect to their mechanism. The activation of a metal surface involves complex phenomena, in which parameters of importance seem to be the hardness and the adhesion of the passivating layer. Some considerations are given on the probable link between sonochemistry and tribochemistry.  相似文献   
12.
Polyethylene oxides are efficient phase transfer catalysts which promote the reduction of CC, CC bonds as well as aromatic substrates by the Na-k eutectic. Yields and general conditions of the reaction give it a generally useful synthetic value.  相似文献   
13.
Organozinc reagents, prepared by sonication from organic halides, lithium and zinc bromide, add conjugatively to α-enals in the presence of nickel acetylacetonate. Satisfactory yields are obtained from arylbromides.  相似文献   
14.
15.
Polyethylene oxides are shown to promote an efficient dihalocarbene formation from bromo — and chloroform and solid potassium hydroxide — Adducts with olefins are obtained in High yields.  相似文献   
16.
A significant improvement in the Wittig-Horner synthesis of allenyl sulfones and allene carboxanilides is described under ultrasonic irradiation in a homogeneous phase.  相似文献   
17.
A new kind of chiral dienophiles, cyclic vinyl-p-tolylsulfilimines (2a and 2b), were obtained from the corresponding (Z)-sulfinylacrylonitriles with HBF(4) and methanol. The asymmetric Diels-Alder reaction of optically pure 2a with cyclopentadiene under mild thermal or catalyzed conditions afforded only the endo-4a adduct with complete endo and pi-facial selectivities. The ability of the sulfilimine moiety to enhance the dienophilic reactivity of the double bond is similar to that of the sulfinyl group.  相似文献   
18.
The zeros in the complex z plane of the Whittaker function Wc/z,µ(z),closely related to spherical waves in the quantum-mechanicalCoulomb problem, are investigated for varying real values ofthe parameters c and µ  相似文献   
19.
Semiempirical MO calculations are shown to provide a more detailed picture of the radical ion mechanism of the Barbier reaction in the general case. Calculated electron affinities give a clue for its extension to other cases.  相似文献   
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