Directed ortho-lithiation of lithium thiophenolate. New methodology for the preparation of ortho-substituted thiophenols and related compounds
GD Figuly, CK Loop, JC Martin
Index: Figuly,G.D.; Loop,C.K.; Martin,J.C. Journal of the American Chemical Society, 1989 , vol. 111, p. 654
Full Text: HTML
Citation Number: 113
Abstract
Abstract: The directed ortho-lithiation of lithium thiophenolate by reaction with n-butyllithium in cyclohexane with N, N,-N', N'-tetramethylethylenediamine gives almost quantitative conversion to lithium 2-lithiobenzenethiolate (1). Reactions of this dilithio derivative with a variety of electrophiles (DzO, carbon dioxide, acetone, diphenyl disulfide, methyl iodide, and thioxanthone) are described. The adduct to thioxanthone is ring-closed to form a ...
Related Articles:
[Shimizu, Daisuke; Takeda, Nobuhiro; Tokitoh, Norihiro Journal of Organometallic Chemistry, 2007 , vol. 692, # 13 p. 2716 - 2728]
Neighboring sulfide group in thermal decomposition of aryldiazonium salts
[Benati,L.; Montevecchi,P.C. Journal of Organic Chemistry, 1977 , vol. 42, p. 2025 - 2028]