The reactions of some α-halo-β-ketosulfones with hard and soft nucleophiles. A preparation of sulfinate esters
JS Grossert, PK Dubey…
Index: Grossert, J. Stuart; Dubey, Pramod K.; Elwood, Tom Canadian Journal of Chemistry, 1985 , vol. 63, p. 1263 - 1267
Full Text: HTML
Citation Number: 21
Abstract
The α-halo-β-ketosulfonyl functionality was attacked by ethanethiolate at the halogen which, in the presence of a proton source, usually resulted in reduction to the β-ketosulfone. A range of other soft nucleophiles did not react, whereas hard nucleophiles invariably attacked at the carbonyl, with subsequent cleavage to α-halosulfones. Ambident arylsulfinate anions usually attacked at halogen to form the sulfonyl halide, which reacted with excess sulfinate ...
Related Articles:
[Jiang, Heng; Cheng, Yuanzheng; Zhang, Yan; Yu, Shouyun European Journal of Organic Chemistry, 2013 , # 24 p. 5485 - 5492]
[Kamigata, Nobumasa; Udodaira, Kumiko; Shimizu, Toshio Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 5 p. 783 - 786]
[Lai, Chunbo; Xi, Chanjuan; Jiang, Yanfeng; Hua, Ruimao Tetrahedron Letters, 2005 , vol. 46, # 3 p. 513 - 515]
[Young, David J.; Stirling, Charles J. M. Journal of the Chemical Society. Perkin Transactions 2, 1997 , # 3 p. 425 - 429]
[Powers, Larry J.; Fogt, S. W.; Ariyan, Z. S.; Rippin, D. J.; Heilman, R. D.; Matthews, Richard J. Journal of Medicinal Chemistry, 1981 , vol. 24, # 5 p. 604 - 609]