Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl–heteroaryl compounds. Issue 13 (20th March 2020)

• Record Type: Journal Article
• Authors: Saritha, Rajendhiran; Annes, Sesuraj Babiola; Saravanan, Subramanian; Ramesh, Subburethinam
• Is Part Of: Organic & biomolecular chemistry. Volume 18:Issue 13(2020)
• Page Start: 2510
• Page End: 2515
• Publication Date: 2020-03-20
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/d0ob00282h
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : A highly regioselective, carbazole based electron donor acceptor (EDA) catalyzed synthesis of biaryl and aryl–heteroaryl compounds is described. Abstract : A highly regioselective, carbazole based Electron Donor Acceptor (EDA) catalyzed synthesis of biaryl and aryl–heteroaryl compounds is described. Various indole and carbazole derivatives were screened for the Homolytic Aromatic Substitution (HAS) reaction. Tetrahydrocarbazole (THC) was very efficient for the HAS transformation and proceeded via a complex formation between diazonium salt and electron rich tetrahydrocarbazole. The UV-Vis spectroscopy technique has been used to confirm the complex formation. The in situ generated EDA complex even in a catalytic amount is found to be efficient for the Single Electron Transfer (SET) process without any photoactivation. Biaryl compounds, 2-phenylfuran, 2-phenylthiophene, and 2-phenylpyrrole and bioactive compounds such as dantrolene and canagliflozin have been synthesized in moderate to excellent yields.