Download Artificial Neural Networks: International Workshop IWANN '91 by Panos A. Ligomenides (auth.), Alberto Prieto (eds.) PDF

By Panos A. Ligomenides (auth.), Alberto Prieto (eds.)

Artificial neural networks are vastly parallel interconnected networks ofsimple components that are meant to have interaction with the items of the true international within the similar manner as organic frightened structures do. curiosity in those networks is because of the opinion that they're in a position to practice projects like photo and speech reputation that experience merely been carried out in restricted methods through conventional computing tools. This ebook comprises invited lectures and the whole contributions to the overseas Workshop onArtificial Neural Networks held in Granada, Spain, September 17-19, 1991. The workshop used to be subsidized by means of the IEEE computing device Society, the Spanish organization for Computing and Automatics, and the college of Granada. The contributions have been chosen via a global application committee; the authors of the papers come from 12 nations. The booklet is prepared in six sections, protecting: - Neural community theories and neural versions - organic views - Neural community architectures and algorithms - software program advancements and instruments - implementations - Applications.

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Extra resources for Artificial Neural Networks: International Workshop IWANN '91 Granada, Spain, September 17–19, 1991 Proceedings

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Allyl phosphorodichloridothionate, which is the starting material for esters of this acid, was obtained by Pletz [146] by the addition of sulphur to allyl phosphorodichloridite, and by the treatment of thiophosphoryl chloride with allyl alcohol: CH2 = CHCH20PC12 + Sv * CH2 = CHCH20PSC12 CH2 ■= CHCH2OH+PSCL/* However, unsaturated esters of phosphorothionic acid are, as a rule, synthesized by the addition of sulphur to the corresponding trialkenyl phos­ phite [91, 111, 121]. Triallyl phosphorothionate PS(OCH 2 CH = CH 2 ) 3 [111] P(OCH2CH = CH2)3 + S ► PS(OCH2CH = CH2)3 Finely ground crystalline sulphur (3 • 2 g) was added to triallyl phosphite (20«2g): an exothermic reaction proceeded on mixing, and all the sulphur dissolved.

Triallyl phosphorothionate PS(OCH 2 CH = CH 2 ) 3 [111] P(OCH2CH = CH2)3 + S ► PS(OCH2CH = CH2)3 Finely ground crystalline sulphur (3 • 2 g) was added to triallyl phosphite (20«2g): an exothermic reaction proceeded on mixing, and all the sulphur dissolved. Distillation afforded triallyl phosphorothionate (18- 87 g, 80-6%), b. p . 125-127°/9 mm, n]? 14832, d™ 1-0827. The 3-chloropropenyl esters of dialkyl hydrogen phosphorothiolothionates were obtained by Tichy [147] by the reaction of salts of these acids with l,3-dichlorobut-2-ene and soda.

P. 93-94°/l mm, 7i2^ 1 ^4500, df 1-0815. Allyl phosphorodichloridothionate, which is the starting material for esters of this acid, was obtained by Pletz [146] by the addition of sulphur to allyl phosphorodichloridite, and by the treatment of thiophosphoryl chloride with allyl alcohol: CH2 = CHCH20PC12 + Sv * CH2 = CHCH20PSC12 CH2 ■= CHCH2OH+PSCL/* However, unsaturated esters of phosphorothionic acid are, as a rule, synthesized by the addition of sulphur to the corresponding trialkenyl phos­ phite [91, 111, 121].

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