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)
Stereoselective synthesis of pyrano[3,2-c]- and furano[3,2-c]quinolines: Gadolinium chloride catalyzed one-pot aza-Diels-Alder reactions
Yu, Yong,Zhou, Jun,Yao, Zhigang,Xu, Fan,Shen, Qi
, p. 351 - 354 (2011/04/22)
A simple and efficient method for the cis-selective synthesis of pyrano- and furano[3,2-c]quinolines via gadolinium chloride catalyzed onepot aza-Diels-Alder reaction is described. Solvent conditions played amajor role in affecting the diastereoselectivity of the products.