4,4,6-trimethyl-2-vinyl-1,3,2-dioxaborinane: An efficient and selective 2-carbon building block for vinylboronate Suzuki-Miyaura coupling reactions

Lightfoot, A.P.; Twiddle, S.J.R.; Whiting, A.

Abstract

An extremely simple and efficient palladium-catalyzed coupling procedure for the synthesis of functionalized styrenes and dienes is utilized to demonstrate how 4,4,6-trimethyl-2-vinyl-1,3,2-dioxaborinane can be employed to selectively undergo Suzuki-Miyaura coupling with a range of halide substrates.

Citation

Lightfoot, A., Twiddle, S., & Whiting, A. (online). 4,4,6-trimethyl-2-vinyl-1,3,2-dioxaborinane: An efficient and selective 2-carbon building block for vinylboronate Suzuki-Miyaura coupling reactions. Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, 529-531

• Journal Article Type: Article
• Journal: Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry
• Print ISSN: 0936-5214
• Electronic ISSN: 1437-2096
• Publisher: Thieme Gruppe
• Peer Reviewed: Peer Reviewed
• Issue: 3
• Pages: 529-531
• Public URL: https://durham-repository.worktribe.com/output/1601603