Iodine-catalyzed synthesis of benzoxazoles using catechols, ammonium acetate, and alkenes/alkynes/ketones via C-C and C-O bond cleavage

6Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

An efficient metal-free synthesis strategy of benzoxazoles was developed via coupling catechols, ammonium acetate, and alkenes/alkynes/ketones. The developed methodology represents an operationally simple, one-pot and large-scale procedure for the preparation of benzoxazole derivatives using molecular iodine as the catalyst.

Cite

CITATION STYLE

APA

Aboonajmi, J., Panahi, F., Hosseini, M. A., Aberi, M., & Sharghi, H. (2022). Iodine-catalyzed synthesis of benzoxazoles using catechols, ammonium acetate, and alkenes/alkynes/ketones via C-C and C-O bond cleavage. RSC Advances, 12(32), 20968–20972. https://doi.org/10.1039/d2ra03340b

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free