Synthesis of Triarylmethanes via Palladium-Catalyzed Suzuki Coupling of Trimethylammonium Salts and Arylboronic Acids was written by Zhang, Zhenming;Wang, Hui;Qiu, Nianli;Kong, Yujing;Zeng, Wenjuan;Zhang, Yongquan;Zhao, Junfeng. And the article was included in Journal of Organic Chemistry in 2018.Application of 113893-08-6 This article mentions the following:
An efficient palladium-catalyzed Suzuki coupling of 1,1-diarylmethyl-trimethylammonium triflates with arylboronic acids is reported. This reaction offers a novel approach to triarylmethane derivatives in good to excellent yields with the palladium-catalyzed C-N bond cleavage as the key feature. Broad substrate scope regarding both reaction partners are observed Moreover, reactive functional groups such as vinyl and formyl groups are conserved in this transformation. In the experiment, the researchers used many compounds, for example, Benzo[b]thiophen-3-ylboronic acid (cas: 113893-08-6Application of 113893-08-6).
Benzo[b]thiophen-3-ylboronic acid (cas: 113893-08-6) belongs to benzothiophene derivatives. Benzothiophene is relatively a stable molecule. The core structure is a part of various pharmaceutical substances and natural products. It has been used as a raw material for the synthesis of biologically active structures and is found in pharmaceuticals such as leukotriene synthesis inhibitors and antifungals, as well as in many natural products.Application of 113893-08-6
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem