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Please use this identifier to cite or link to this item: http://hdl.handle.net/2241/103916

Title: Efficient Synthesis of Thiobenzanilides by Willgerodt-Kindler Reaction with Base Catalysts
Authors: Okamoto, Ken
Yamamoto, Takakazu
Kanbara, Takaki
神原, 貴樹
Issue Date: Oct-2007
Publisher: Georg Thieme Verlag
Journal Title: Synlett
Volume: 2007
Issue: 17
Start Page: 2687
End Page: 2690
DOI: 10.1055/s-2007-991073
Abstract: Willgerodt-Kindler reaction between anilines and benz­aldehydes readily proceeded in the presence of catalytic amount of Na2S·9H2O to give thiobenzanilides in moderate to good yields. The base catalyst was also available for preparation of primary thio­benzamide.
URI: http://hdl.handle.net/2241/103916
Rights: © Georg Thieme Verlag Stuttgart · New York
Text Version: author
Appears in Collections:Synlett
神原 貴樹 (Kanbara Takaki)

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