A Cycloaddition Reaction of Benzyne
HE Simmons
Index: Simmons,H.E. Journal of the American Chemical Society, 1961 , vol. 83, p. 1657 - 1664
Full Text: HTML
Citation Number: 86
Abstract
Introduction.-The electrically neutral intermediate benzyne (CEH4) l is highly reactive when prepared under a variety of conditions. 2 The kinds of reactions undergone by benzyne that have been distinguished thus far include facile attack by dimerization and trimerization, 6 and Diels-Alder addition. jS6 The observed products and the conditions under which many of these reactions occur indicate that benzyne is one of the most highly reactive ...
Related Articles:
A New Route to 1, 3-Dienes: TMSI Elimination of 2-Ene-1, 4-diols
[Hill, Richard K.; Pendalwar, Shekhar L.; Kielbasinski, Karen; Baevsky, Matthew F.; Nugara, Peter N. Synthetic Communications, 1990 , vol. 20, # 12 p. 1877 - 1884]
[Hussain, Abid; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.; Gao, Yaping Journal of Organic Chemistry, 1993 , vol. 58, # 13 p. 3578 - 3581]
[Hussain, Abid; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.; Gao, Yaping Journal of Organic Chemistry, 1993 , vol. 58, # 13 p. 3578 - 3581]
[Cristol, Stanley J.; Klein, Michael W.; Hendewerk, Monica H.; Daussin, Rory D. Journal of Organic Chemistry, 1981 , vol. 46, # 24 p. 4992 - 4998]
[Morrison, Harry; Muthuramu, Kayambu; Pandey, Genesh; Severance, Daniel; Bigot, Bernard Journal of Organic Chemistry, 1986 , vol. 51, # 17 p. 3358 - 3363]