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ChemInform Abstract: Novel Pathways in the Reactions of Vinylsilanes with Lithium Metal

✍ Scribed by A. MAERCKER; K. REIDER; U. GIRRESER

Publisher
John Wiley and Sons
Year
2010
Weight
24 KB
Volume
29
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES

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Vinylsilanes are known to react with lithium metal to form lithium hydride, either a 1,4-proton shift of 25 to 26 or a Grovenstein-Zimmerman rearrangement of 45 to 47 can either 1,2-dilithioethanes by reduction or 1,4-dilithiobutanes by reductive dimerization. The reaction of the substituted occur a

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Reactions of Thioamides with Metal Carboxylates in Organic Media. -Treatment of thioamides with Ag(I)-and Hg(II)-carboxylates results in simple and efficient formation of nitriles, imides, or amides depending on the substitution pattern of thioamides.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v