A mild and highly efficient one-pot three-component reaction for carbon–sulfur bond formation catalyzed by potassium tert-butoxide
B Movassagh, A Rakhshani
Index: Movassagh, Barahman; Rakhshani, Amir Chinese Chemical Letters, 2011 , vol. 22, # 10 p. 1179 - 1182
Full Text: HTML
Citation Number: 7
Abstract
Potassium tert-butoxide has been found to be a highly efficient catalyst for one-pot, three- component reaction of aryl aldehydes, acetophenones, and thiols via Claisen– Schmidt/Michael addition reactions for the synthesis of thia-Michael adducts in high yields. The reactions are best carried out in tert-butyl alcohol at room temperature.
Related Articles:
[Climent, Maria J.; Iborra, Sara; Sabater, Maria J.; Vidal, Juan D. Applied Catalysis A: General, 2014 , vol. 481, p. 27 - 38]
[Alt, Isabel; Rohse, Philipp; Plietker, Bernd ACS Catalysis, 2013 , vol. 3, # 12 p. 3002 - 3005]
[Dong, Dewen; Yu, Haifeng; Ouyang, Yan; Liu, Qun; Bi, Xihe; Lu, Yumei Synlett, 2006 , # 2 p. 283 - 287]
[Dong, Dewen; Yu, Haifeng; Ouyang, Yan; Liu, Qun; Bi, Xihe; Lu, Yumei Synlett, 2006 , # 2 p. 283 - 287]