Photochemical thiylation of Si-methoxy-substituted 1, 2-disilylethylenes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1976-01

AUTHORS

M. G. Voronkov, L. V. Tsvetaeva, M. V. Sigalov, Z. I. Mikhailov, N. F. Chernov, O. G. Yarosh, V. A. Pestunovich

ABSTRACT

ConclusionsA number of new sulfur-containing organosilicon monomers was synthesized by the reaction of 1,2-bis(alkylmethoxysilyl)- and 1-(trimethylsilyl)-2-(methylmethoxysilyi)ethylenes with mercaptans and thioacetic acid.Based on the NMR spectral data, the 1-(trimethylsilyl)-2-(methylmethoxysilyl)ethylenes form two isomeric adducts in a 1∶1 ratio.

PAGES

160-163

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00925642

DOI

http://dx.doi.org/10.1007/bf00925642

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1036251668


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