Vinyltetrazoles: III. Metal-catalyzed arylation, a new method of vinyltetrazoles functionalization
作者:P. A. Aleshunin、K. A. Esikov、F. M. Dolgushin、V. A. Ostrovskii
DOI:10.1134/s1070428012110097
日期:2012.11
New functionalization procedure was developed for C- and N-vinyltetrazoles based on Heck reaction. Applying this method diverse (E)-styryl- and (E)-distyryltetrazoles were obtained for the first time in 76-85% yields. C-Vinyltetrazoles are more reactive in Heck cross-coupling than N-vinyltetrazoles. The arylation of 1-vinyltetrazole along Heck reaction proceeds with a C-H-activation and leads to the formation of 5-phenyl-1-[2-(E)-phenylethenyl]tetrazole.
CASEY, M.;MOODY, C. J.;REES, C. W., J. CHEM. SOC. CHEM. COMMUN., 1982, N 13, 714-715
作者:CASEY, M.、MOODY, C. J.、REES, C. W.
DOI:——
日期:——
CASEY, M.;MOODY, CH. J.;REES, CH. W., J. CHEM. SOC. PERKIN TRANS., 1984, N 8, 1933-1941
作者:CASEY, M.、MOODY, CH. J.、REES, CH. W.
DOI:——
日期:——
Casey, Michael; Moody, Christopher J.; Rees, Charles W., Journal of the Chemical Society. Perkin transactions I, 1984, # 8, p. 1933 - 1941
作者:Casey, Michael、Moody, Christopher J.、Rees, Charles W.