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 MoreSynochem Ingredients Corp., Ltd.
Contact:+86-512-5636 2180
Address:Zhangjiagang Free Trade Zone
ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.
website:http://www.zenvasino.com
Contact:+86-138-72658998
Address:Shibeishan Road,Zhijiang, Hubei, China
Contact:86 513 85512619
Address:Rm.1306, Building A, Wenfeng Mansion,168 Gongnong Road, Nantong Jiangsu China
Contact:+86-511-88790000
Address:338 North Yushan Rd, Zhenjiang, Jiangsu 212016
website:http://www.acrospharmatech.com
Contact:+1-3234804688
Address:Flat/RM 1502,Easey Commercial building 253-261 Hennessy Road,Wanchai，HongKong
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)
