Intramolecular C–H Functionalization of α-Alkyl-α-diazoesters toward the Synthesis of Lactones
), a sterically bulky achiral catalyst, was found to enable the formation of lactones. Alkyl γ-lactones were synthesized in excellent yields and diastereoselectivity, and a diverse array of disubstituted lactones (γ, δ, and ε) were synthesized with good yields and diastereoselectivity. This chemistry was extended to intramolecular C-H insertion in late-stage functionalization with excellent regio- and diastereoselectivity.
Authors
- Bijaya Bagale (ORCID: https://orcid.org/0009-0001-3424-0761)
- Jeffrey D. Mighion (ORCID: https://orcid.org/0000-0001-6908-5186)
- Aubree Nolan
- Elizabeth U. Heuser
Institutions
- Kent State University (US)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-05-12
- DOI
- https://doi.org/10.1021/acs.orglett.6c01332
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Kent State University