Issue 6, 2000

Synthesis and ring enlargement of 2-ethoxycarbonyl-1-silacyclobutanes

Abstract

2-Ethoxycarbonyl-1-silacyclobutanes were synthesized by intramolecular C–H insertion of carbenes generated photochemically from α-(di-tert-butylsilyl)-α-diazoacetates; they undergo smooth thermal ring-expansion by a 1,3(C → O) silyl shift to form 6-ethoxy-1-oxa-2-silacyclohex-5-enes.

Article information

Article type
Communication
Submitted
23 Nov 1999
Accepted
04 Feb 2000
First published
03 Mar 2000

Chem. Commun., 2000, 437-438

Synthesis and ring enlargement of 2-ethoxycarbonyl-1-silacyclobutanes

G. Maas and S. Bender, Chem. Commun., 2000, 437 DOI: 10.1039/A909306K

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