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Organometallic derivatives of furan. LII. Synthesis of carbofunctional furylsilanes and their /sup 1/H, /sup 13/C, and /sup 29/Si NMR spectroscopic and quantum-chemical investigation

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5676700

Under the standard conditions for the synthesis of furan compounds it is possible to obtain the carbofunctional derivatives of silylated furfural with retention of the trimethylsilyl group in the ring. By NMR and CNDO/2 LCAO MO methods and also as a result of the investigation of the chemical characteristics of silylated furfural and its carbofunctional derivatives it was established that the introduction of a trimethylsilyl group at position 5 of the furan ring does not change the reactivity of the carbofunctional substituents at position 2. The electronic effects of the substituents are hardly transmitted through the furan ring at all. The effect of substituents in the carbofunctional furylsilanes on the electronic structure of the ring is additive.

Research Organization:
Institute of Organic Synthesis, Riga, USSR
OSTI ID:
5676700
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 55:9; ISSN JGCHA
Country of Publication:
United States
Language:
English

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