637348-15-3Relevant academic research and scientific papers
Regio- and Stereoselective Electrophilic Cyclization Approach for the Protecting-Group-Free Synthesis of Alkaloids Lennoxamine, Chilenine, Fumaridine, 8-Oxypseudoplamatine, and 2- O-(Methyloxy)fagaronine
Yao, Tuanli,Guo, Zhen,Liang, Xiujuan,Qi, Lihan
, p. 13370 - 13380 (2018/10/24)
A unified strategy for protecting-group-free synthesis of alkaloids lennoxamine, chilenine, fumaridine, 8-oxypseudoplamatine, and 2-O-(methyloxy)fagaronine is reported. The core isoindolin-1-one and isoquinolin-1-one structures were built by a silver-cata
Gold-facilitated '6-exo-dig' intramolecular cyclization of 2-[(2-nitrophenyl)ethynyl]phenylacetic acids: General access to 5H-benzo[b]carbazole-6,11-diones
Salas, Cristian O.,Reboredo, Francisco J.,Estevez, Juan C.,Tapia, Ricardo A.,Estevez, Ramon J.
scheme or table, p. 3107 - 3110 (2010/03/02)
The preliminary results of a regiospecific synthesis of (Z)-1 -(2-nitrobenzylidene)isochroman-3-ones by gold(I)-catalyzed cycloisomerization of phenylethynylacetic acids under mild conditions is described. These novel lactones proved to be suitable starti
Copper(I) mediated intramolecular cyclization of 2-(2-amino-phenylethynyl)benzoic and [2-(2-aminophenylethynyl)phenyl]acetic acid esters: A new synthetic step towards isoindolo[2,1-a]indoles and 5H-indolo[2,1-a]isoquinolines
Reboredo, Francisco J.,Treus, Mónica,Estévez, Juan C.,Castedo, Luis,Estévez, Ramón J.
, p. 1603 - 1606 (2007/10/03)
We describe herein parallel synthetic routes to isoindolo[2,1-a]indoles and 5H-indolo[2,1-a]isoquinolines from 2-(2-aminophenylethynyl)benzoic acid esters and [2-(2-aminophenylethynyl)phenyl]acetic acid esters, respectively.
