An article Light-induced metal-free transformations of unactivated pyridotriazoles WOS:000487086900012 published article about CATALYZED DENITROGENATIVE TRANSANNULATION; N-SULFONYL AZIDES; TERMINAL ALKYNES; DIASTEREOSELECTIVE SYNTHESIS; AZAVINYL CARBENES; DIRECT ARYLATION; REACTIVITY; N-SULFONYL-1,2,3-TRIAZOLES; 1,2,3-TRIAZOLES; ANNULATION in [Zhang, Ziyan; Yadagiri, Dongari; Gevorgyan, Vladimir] Univ Illinois, Dept Chem, 845 W Taylor St, Chicago, IL 60607 USA; [Zhang, Ziyan; Yadagiri, Dongari; Gevorgyan, Vladimir] Univ Texas Dallas, Dept Chem & Biochem, 800 W Campbell RD, Richardson, TX 75080 USA in 2019, Cited 95. Formula: C7H5F3O. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9
A highly efficient and practical method for incorporation of the arylmethylpyridyl moiety into diverse molecules has been developed. This method features the transition metal-free light-induced room temperature transformation of pyridotriazoles into pyridyl carbenes, which are capable of smooth arylation, X-H insertion, and cyclopropanation reactions. The synthetic usefulness of the developed method was illustrated in a facile synthesis of biologically active molecules.
Welcome to talk about 98-17-9, If you have any questions, you can contact Zhang, ZY; Yadagiri, D; Gevorgyan, V or send Email.. Formula: C7H5F3O
Reference:
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