Treuerne Balazs, Krisztina E.; Molnar, Mark; Madarasz, Zoltan; Nyerges, Miklos published the artcile< A facile synthesis of novel polycyclic spiropyrrolidine oxindoles incorporating the 1,3-dipolar cycloaddition of azomethine ylides>, Product Details of C8H6ClNO, the main research area is polycyclic spiropyrrolidine oxindole preparation regio diastereoselective; azomethine ylide arylmethylene indolinone dipolar cycloaddition.
This study describes the synthesis of novel polycyclic spiropyrrolidine oxindoles through the 1,3-dipolar cycloaddition of azomethine ylides generated in situ with 3-(arylmethylene)-indolin-2-ones. Effect of substituents of azomethine ylides and various dipolarophiles on reactivity, as well as on the products regio- and stereoselectivity was investigated.
Synthetic Communications published new progress about 1,3-Dipolar cycloaddition reaction, regioselective. 20870-77-3 belongs to class indole-building-block, and the molecular formula is C8H6ClNO, Product Details of C8H6ClNO.
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles