771477-53-3Relevant academic research and scientific papers
Bu4N[AuCl4]-catalyzed synthesis of highly substituted furans from 2-(1-alkynyl)-2-alken-1-ones in ionic liquids: An air-stable and recyclable catalytic system
Liu, Xueyuan,Pan, Zhenliang,Shu, Xingzhong,Duan, Xinhua,Liang, Yongmin
, p. 1962 - 1964 (2006)
The cyclization of 2-(1-alkynyl)-2-alken-1-ones proceeded smoothly in the presence of various nucleophiles with a catalytic amount of Bu 4N[AuCl4] in [bmim]BF4, leading to the formation of highly substituted furans. This s
Nucleophile-assisted Pt-catalyzed cyclization of enynones: an access to synthesis of highly substituted furans
Oh, Chang Ho,Reddy, V. Raghava,Kim, Ahyun,Rhim, Chul Yun
, p. 5307 - 5310 (2006)
A new and efficient Pt-catalyzed hydroxy- or alkoxy cyclization of 2-(1-alkynyl)-2-alkene-1-ones offers a general synthetic pathway to a wide range of highly substituted furans in good to excellent yields.
Cu(I) catalyst in DMF: An efficient catalytic system for the synthesis of furans from 2-(1-alkynyl)-2-alken-1-ones
Patil, Nitin T.,Wu, Huanyou,Yamamoto, Yoshinori
, p. 4531 - 4534 (2005)
The cyclization of 2-(1-alkynyl)-2-alken-1-ones 1 proceeded very smoothly in the presence of alcohols 2 with a catalytic amount of Cu(I)Br in DMF at 80 °C, leading to the formation of highly substituted furans 3. The catalytic system reported herein is ea
AuCl3-catalyzed synthesis of highly substituted furans from 2-(1-alkynyl)-2-alken-1-ones
Yao, Tuanli,Zhang, Xiaoxia,Larock, Richard C.
, p. 11164 - 11165 (2007/10/03)
Highly substituted furans have been synthesized by the reaction of 2-(1-alkynyl)-2-alken-1-ones and various nucleophiles under very mild reaction conditions in good to excellent yields. Gold and some other transition metals are efficient catalysts for thi
