Simple, one-step syntheses of tri- and tetracyclic B,N,S-heterocycles from reactions of a diboracumulene with thiols
Boron-containing fused heterocycles have received considerable attention due to their unique structures, bonding, and intriguing properties. However, progress in this area has been hampered by a lack of efficient synthetic methodologies. In this study, we demonstrate the reactivity of a diboracumulene, LBBL (L = cyclic (alkyl)(amino)carbene, CAAC), with various nitrogen-containing heterocyclic thiols. These straightforward reactions result in the partial or complete cleavage of the B-B multiple bonds in the diboracumulene, along with S-H bond activation in the thiol units, leading to the formation of a range of tricyclic and tetracyclic B,N,S-heterocycles. Notably, the tricyclic B,N,S-heterocycle exhibits π aromaticity in all three of its rings.
Authors
- Rian D. Dewhurst (ORCID: https://orcid.org/0000-0001-5978-811X)
- Christian Markl
- Holger Braunschweig (ORCID: https://orcid.org/0000-0001-9264-1726)
- Sourav Kar (ORCID: https://orcid.org/0000-0001-7477-7494)
- Kai Hammond
- Lukas Lubczyk
Institutions
- University of Würzburg (DE)
Publication Details
- Journal
- Chemical Science
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5sc04751j
- Citations
- 1
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- Alexander von Humboldt-Stiftung