Journal of the Chemical Society (Resumed)

124. The synthesis of some p-arylsulphonylbenzaldehydes and related aldehydes and ketones

H Burton, PF Hu

Index: Burton; Hu Journal of the Chemical Society, 1948 , p. 601

Full Text: HTML

Citation Number: 12

Abstract

Representative p-arylsulphonylbenzaldehydes were obtained by the route, Ar* SO,* C, H, Me __f Ar* SO,* C, H,~ CH (OAc),--+ Ar* SO, C, H, CHO, provided that the group Ar was not susceptible to oxidation by chromic oxide. Related aldehydes and ketones were prepared by standard methods. Phenyl thiolacetate, PhSAc, did not undergo the Fries rearrangement or the Friedel-Crafts reaction, but the latter method was successful with thioanisole.

Related Articles:

Quinone dehydrogenation. Oxidation of benzylic alcohols with 2, 3-dichloro-5, 6-dicyanobenzoquinone

[Becker, Hans-Dieter; Bjoerk, Anders; Adler, Erich Journal of Organic Chemistry, 1980 , vol. 45, # 9 p. 1596 - 1600]

Non-basic ligands for aminergic GPCRs: The discovery and development diaryl sulfones as selective, orally bioavailable 5-HT 2A receptor antagonists for the …

[Ladduwahetty, Tammy; Gilligan, Myra; Humphries, Alexander; Merchant, Kevin J.; Fish, Rebecca; McAlister, George; Ivarsson, Magnus; Dominguez, Maria; O'Connor, Desmond; MacLeod, Angus M. Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 12 p. 3708 - 3712]

More Articles...