File:Oxidation of thiophene with trifluoroperacetic acid.png

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摘要

描述	w:Thiophene is oxidised by w:trifluoroperacetic acid by two pathways. The major reaction involves the formation of thiophene-S-oxide which undergoes subsequent w:Diels-Alder-style dimerisation and further oxidation. The minor pathway involves the formation of thiophene-2,3-epoxide and subsequent rearrangement to thiophene-2-one. The reaction is discussed in the paper doi: doi:10.1021/jo0202177 and in the w:Encyclopedia of Reagents for Organic Synthesis article at doi: doi:10.1002/047084289X.rt254.pub2 . The image was extracted and modified from this PDF of the EROS manuscript by w:user:EdChem and uploaded to Wikipedia on the same day. Whilst the EROS content is copyright protected, individual chemical structures and equations are ineligible for such protection.
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日期/时间	大小	用户	备注
2017-01-22 00:11:43	833× 450×	EdChem	[[Thiophene]] is oxidised by [[trifluoroperacetic acid]] by two pathways. The major reaction involves the formation of thiophene-''S''-oxide which undergoes subsequent [[Diels-Alder]]-style dimerisation and further oxidation. The minor pathway involv...