Reactivity of thiazole in electrophilic reactions as determined from solvolysis rates
DS Noyce, SA Fike
Index: Noyce,D.S.; Fike,S.A. Journal of Organic Chemistry, 1973 , vol. 38, p. 3316 - 3318
Full Text: HTML
Citation Number: 22
Abstract
The solvolysis of a-arylethanol derivatives is a useful probe of aromatic reactivity. Streitwieser, et aZ., 2-4 have recently compared the reactivities of a large number of aromatic hydrocarbons, and the sol-volysis rates of the corresponding arylmethyl tosylates. There is good correspondence in the two series, covering a wide variety of types and conditions12 and to various semiempirical AI0 meth~ ds;~ the results lead to a useful set ...
Related Articles:
1, 2, 3-triazolo [5, 1-b] thiazoles; synthesis and properties
[Jones, Gurnos; Ollivierre, Hermione; Fuller, L. S.; Young, J. H. Tetrahedron, 1991 , vol. 47, # 16 p. 2851 - 2860]
Efficient chemoenzymatic dynamic kinetic resolution of 1-heteroaryl ethanols
[Allevi, Pietro; Ciuffreda, Pierangela; Tarocco, Giorgio; Anastasia, Mario Journal of Organic Chemistry, 1996 , vol. 61, # 12 p. 4144 - 4147]
[Jones, Gurnos; Ollivierre, Hermione; Fuller; Young Tetrahedron, 1991 , vol. 47, # 16-17 p. 2861 - 2870]
1, 2, 3-triazolo [5, 1-b] thiazoles; synthesis and properties
[Jones, Gurnos; Ollivierre, Hermione; Fuller, L. S.; Young, J. H. Tetrahedron, 1991 , vol. 47, # 16 p. 2851 - 2860]