An article 4-Aminoindoles as 1,4-bisnucleophiles for diversity-oriented synthesis of tricyclic indoles bearing 3,4-fused seven-membered rings WOS:000471907500016 published article about ONE-POT SYNTHESIS; FACILE SYNTHESIS; 3-COMPONENT REACTIONS; 4-COMPONENT REACTIONS; EXPEDIENT SYNTHESIS; EFFICIENT SYNTHESIS; CATALYST; HYDROGENATION; PROTOCOL; CASCADE in [Chen, Shaomin; Ravichandiran, Palanisamy; El-Harairy, Ahmed; Li, Minghao; Gu, Yanlong] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Minist Educ, Key Lab Large Format Battery Mat & Syst, Wuhan 430074, Hubei, Peoples R China; [Queneau, Yves] Univ Claude Bernard, Univ Lyon 1, Univ Lyon,INSA Lyon,CPE Lyon,ICBMS, Inst Chim & Biochim Mol & Supramol,CNRS,UMR 5246, Batiment Lederer,1 Rue Victor Grignard, F-69622 Villeurbanne, France; [Gu, Yanlong] Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China in 2019.0, Cited 97.0. Category: thiazolidines. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7
A straightforward access to tricyclic indoles bearing 3,4-fused seven-membered rings has been established by using 4-aminoindoles as 1,4-bisnucleophiles in three-component reactions. 1H-Azepino[4,3,2-cd]indoles, 4,6-dihydro-1H-azepino[4,3,2-cd]indoles and 1,3,4,6-tetrahydro-5H-azepino[4,3,2-cd]indol-5-ones could thus be synthesized in one pot in moderate to good yields. Beyond opening access to 3,4-fused tricyclic indoles, the use of easily accessible 4-aminoindoles as C,N-1,4-bisnucleophiles also provides a new platform to be used in a diversity-oriented synthesis strategy, fully displaying its benefits of maximizing molecular complexity and reaction diversity.
Category: thiazolidines. About Chalcone, If you have any questions, you can contact Chen, SM; Ravichandiran, P; El-Harairy, A; Queneau, Y; Li, MH; Gu, YL or concate me.
Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com