Journal of Physical Chemistry p. 4691 - 4694 (1986)
Update date:2022-08-03
Topics:
Gaspar, Peter P.
Berowitz, David M.
Strongin, Daniel R.
Svoboda, Daniel L.
Tuchler, Matthew B.
et al.
Formation of benzocyclobutene, a characteristic rearrangement product of tolylmethylenes, strongly suggest that these species are formed as intermediates in the reactions of recoiling carbon-11 atoms and toluene.Degradation and additive studies indicated that both singlet and triplet carbon atoms can lead to benzocyclobutene formation through insertion into ring C-H bonds.Styrene is also formed, predominantly by insertion of singlet C-11 atoms into a methyl C-H bond, followed by rearrangement of the resulting benzylmethylene.
View MoreContact:0086 533 2282832
Address:Zibo，Shandong
Hangzhou Yingshanhua Pigment Chemicals Co.,Ltd.
Contact:+86-0150-58101658
Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China
Tianjin Tongde Biological Technology Co., Ltd.
Contact:86-22-23309138
Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
Anqing World Chemical Co., Ltd.
Contact:+86-556-5800026
Address:Daguan Economic Development Zone of circular economy industrial park Anqing City Anhui province
WEIFANG RICHEM INTERNATIONAL LTD
Contact:86-536-2222176
Address:weifang,shandong
Doi:10.1021/om800141y
(2008)Doi:10.1021/jm00161a005
(1986)Doi:10.1016/j.tetlet.2008.04.076
(2008)Doi:10.1021/ja01539a035
(1958)Doi:10.1021/np800185k
(2008)Doi:10.1016/j.saa.2007.10.054
(2008)
