Palladium‐Catalyzed <i>β</i> − Carbonyl Alkylation of <i>α</i> ‐Imino Esters With Allylic/Propargyl Alcohols
ABSTRACT A palladium‐catalyzed β ‐carbonyl alkylation of α ‐imino esters with readily available allylic/propargyl alcohols has been developed, enabling efficient synthesis of structurally diverse δ ‐carbonyl‐ α ‐amino acid esters and carbonyl‐containing pyrrolidine derivatives. Mechanistic studies indicate that the reaction proceeds via a dehydrogenation‐Michael addition or [3 + 2] cyclization pathway. This method offers an atom‐economical and operationally straightforward strategy for the synthesis of highly functionalized Δ(1)‐pyrrolines and pyrrolidines.
Authors
- Lei Bai (ORCID: https://orcid.org/0009-0004-7910-7771)
- Changming Xu
- Sijia Shang
Institutions
- Lanzhou Jiaotong University (CN)
- Northwest Normal University (CN)
Publication Details
- Journal
- Applied Organometallic Chemistry
- Published
- 2026-01-08
- DOI
- https://doi.org/10.1002/aoc.70515
- Primary Topic
- Catalytic Alkyne Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00