Borane-catalyzed dehydrogenative C–C bond formation of indoles with N-tosylhydrazones: an experimental and computational study. Issue 13 (12th May 2022)

• Record Type: Journal Article
• Authors: Dipika, ; Sharma, Yogesh Brijwashi; Pant, Suyash; Dhaked, Devendra Kumar; Guru, Murali Mohan
• Is Part Of: Organic chemistry frontiers. Volume 9:Issue 13(2022)
• Page Start: 3428
• Page End: 3437
• Publication Date: 2022-05-12
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d2qo00552b
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : A novel dehydrogenative C–C bond formation of indoles and N -tosylhydrazones to give di(indolyl)methanes (DIMs) has been demonstrated using tris(pentafluorophenyl)borane as a catalyst. Abstract : A novel dehydrogenative C–C bond formation of indoles and N -tosylhydrazones to give di(indolyl)methanes (DIMs) has been demonstrated using tris(pentafluorophenyl)borane as a catalyst. A wide range of functional groups can be tolerated under this metal-free protocol to afford symmetrical and most importantly unsymmetrical DIMs. Extensive experimental investigations like the kinetic profile, Hammett plot, determination of reaction order, and HRMS analysis for intermediates along with computational study suggest that the reaction proceeds through sequential intermolecular C–C/C–C bond formation with indoles and borane adducts of N -tosylhydrazones followed by acceptorless dehydrogenation for the access of bioactive DIMs.