107933-56-2Relevant articles and documents
One-pot regioselective vinylation of tetrazoles: preparation of 5-substituted 2-vinyl-2H-tetrazoles
Roh, Jaroslav,Vávrová, Kate?ina,Hrabálek, Alexandr
experimental part, p. 1411 - 1414 (2010/04/25)
The one-pot regioselective preparation of 5-aryl/alkyl-2-vinyl-2H-tetrazoles from 5-substituted tetrazoles via a very simple procedure using 1,2-dibromoethane and triethylamine without the need of any catalyst is described. The mechanism of this reaction is also discussed.
SYNTHESIS OF FUNCTIONALLY SUBSTITUTED N-VINYLTETRAZOLES
Vereshchagin, L. I.,Buzilova, S. R.,Mityukova, T. K.,Proidakov, A. G.,Kizhnyaev, V. N.,et al.
, p. 1777 - 1783 (2007/10/02)
5-Alkyl- and 5-aryl-N-vinyltetrazoles (II) are formed during vinyl exchange between 5-substituted tetrazoles (I) and vinyl acetate in the presence of the copper acetate-boron trifluoride etherate catalytic system.The direction of vinylation depends on steric effects and on the electronic nature of the substituents at position 5 of the tetrazole ring.A series of functionally substituted 2-vinyltetrazoles were obtained by nucleophilic substitution of the chlorine in 2-vinyl-5-chloromethyltetrazole.