From acyl boronates to functional boronate-substituted and boron-containing heterocycles: emerging methods and applications

Abstract

Over the past decade, acyl boronates have emerged as versatile and valuable precursors in organic synthesis, facilitating the construction of diverse and important classes of compounds. In this review, we highlight a growing application of acyl boronates that has gained significant traction in recent years, namely, their use in the regioselective construction of boronate-substituted or boron-containing heterocyclic motifs. This approach leverages the unique bifunctional nature of acyl boronates, which combines the reactivity of both the boron moiety and the carbonyl group within the same molecule. Particular emphasis is placed on the structural diversity and synthetic utility of these compounds, as well as their emerging roles in both synthetic organic chemistry and materials science.

Graphical abstract: From acyl boronates to functional boronate-substituted and boron-containing heterocycles: emerging methods and applications

Article information

Article type
Highlight
Submitted
20 Nov 2025
Accepted
08 Jan 2026
First published
09 Jan 2026

Org. Chem. Front., 2026, Advance Article

From acyl boronates to functional boronate-substituted and boron-containing heterocycles: emerging methods and applications

K. Gosak and Z. Časar, Org. Chem. Front., 2026, Advance Article , DOI: 10.1039/D5QO01583A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements