1212160-10-5Relevant articles and documents
Stereoselective synthesis of pyrano[3,2-c]- and furano[3,2-c]quinolines: Samarium diiodide-catalyzed one-pot aza-Diels-Alder reactions
Zhou, Zhuqing,Xu, Fan,Han, Xiaoyan,Zhou, Jun,Shen, Qi
, p. 5265 - 5269 (2007)
Three-component aza-Diels-Alder reactions involving aromatic aldehydes, aromatic amines, and dihydropyran or dihydrofuran are effectively catalyzed by samarium diiodide to afford pyrano[3,2-c]- or furano[3,2-c]quinolines in good yields and with high stere
Ceric Ammonium Nitrate (CAN)-Catalyzed, Efficient, One-Pot, Three-Component, aza-Diels-Alder Reactions for a Facile Synthesis of Tetrahydropyranoquinoline Derivatives
Puligoundla, Ravinder Goud,Vulupala, Hanmanth Reddy,Kommu, Nagaiah,Kondra, Sudhakar Babu
supporting information, p. 504 - 512 (2015/10/29)
A simple, efficient, and cost-effective method for the synthesis of tetrahydropyranoquinoline derivatives by a one-pot condensation of aromatic aldehyde, aromatic amine, and 3,4-dihydro-2H-pyran respectively in the presence of ceric ammonium nitrate (CAN)
Samarium triflate as mild and efficient catalyst for aza-diels-alder reaction: A facile synthesis of cis-fused pyrano-and furanoquinolines
Narsaiah, A. Venkat,Reddy, A. Ramesh,Reddy, B. V. Subba,Yadav
experimental part, p. 1750 - 1757 (2010/07/05)
Three-component coupling reactions of aldehydes, amines, and cyclic enol ethers have been carried out in the presence of samarium triflate to afford the corresponding pyrano and furanoquinolines in excellent yields with high endo-selectivity. The reaction