The important role of Ranitidine

Related Products of 66357-35-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 66357-35-5.

Related Products of 66357-35-5, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 66357-35-5, Name is Ranitidine, SMILES is O=[N+]([O-])/C=C(NCCSCC1=CC=C(O1)CN(C)C)NC, belongs to benzofurans compound. In a article, author is Laxmikeshav, Kritika, introduce new discover of the category.

Microwave-Assisted Regioselective Friedel-Crafts Arylation by BF3 . OEt2: A Facile Synthetic Access to 3-Substituted-3-Propargyl Oxindole Scaffolds

A facile microwave-assisted synthetic strategy for the construction of C-C bondviaregioselective Friedel-Crafts arylation of 3-hydroxy-3-phenylethynyl oxindoles with different electron-rich nucleophiles such as phenols, sulphonamides, anisole, benzofuran, and benzothiophene has been established by employing BF3 . OEt(2)as catalyst. The current protocol attributes mild conditions, cost-effective, transition-metal free synthesis, wide substrate scope and moderate to good yields. Moreover, this method is amenable for the generation of a library of densely substituted 3-(4-hydroxyphenyl)-3-(phenylethynyl) oxindoles and 3-(4-benzenesulphonamide)-3-(phenylethynyl) oxindoles as privileged scaffolds.

Related Products of 66357-35-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 66357-35-5.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem