Metalation reactions. XXIV. Metalation of (vinylthio) benzene
…, S Cabiddu, E Cadoni, R Cannas, C Fattuoni, S Melis
Index: Cabiddu, Maria Grazia; Cabiddu, Salvatore; Cadoni, Enzo; Cannas, Rita; Fattuoni, Claudia; Melis, Stefana Tetrahedron, 1998 , vol. 54, # 46 p. 14095 - 14104
Full Text: HTML
Citation Number: 8
Abstract
The addition of organolithium compounds to (vinylthio) benzene (1) and then an electrophilic quenching followed by a further metalation/electrophilic quenching is a general method to prepare in one pot (alkylthio) benzenes ortho, alpha-substituted with equal or different groups. The direct dimetalation of 1 affords the ortho, alpha-dilithiated species 15 besides other by-products. Starting from 15 it is possible to obtain in one step ortho, alpha- ...
Related Articles:
[Fernandez-Rodriguez, Manuel A.; Shen, Qilong; Hartwig, John F. Chemistry - A European Journal, 2006 , vol. 12, # 30 p. 7782 - 7796]
[Scholz, Roland; Hellmann, Gunther; Rohs, Susanne; Raabe, Gerhard; Runsink, Jan; Oezdemir, Diana; Luche, Olaf; Hess, Thomas; Giesen, Alexander W.; Atodiresei, Juliana; Lindner, Hans J.; Gais, Hans-Joachim European Journal of Organic Chemistry, 2010 , # 24 p. 4559 - 4587]
[Cohen,T.; Ritter,R.H.; Oulette,D. Journal of the American Chemical Society, 1982 , vol. 104, p. 7142]
[Harada, Toshiro; Maeda, Hisatomo; Oku, Akira Tetrahedron Letters, 1985 , vol. 26, # 52 p. 6489 - 6492]
The Rearrangement of Alkyl Aryl Thioethers
[Taylor Journal of the American Chemical Society, 1936 , vol. 58, p. 2649,2650]