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.

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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
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article

Palladium‐Catalyzed β  − Carbonyl Alkylation of α ‐Imino Esters With Allylic/Propargyl Alcohols

Lei Bai, Changming Xu, Sijia Shang
Applied Organometallic Chemistry
Catalytic Alkyne Reactions
article

Palladium‐Catalyzed β  − Carbonyl Alkylation of α ‐Imino Esters With Allylic/Propargyl Alcohols

Lei Bai, Changming Xu, Sijia Shang
article en

Abstract

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.

Applied Organometallic ChemistryVol. 40(2)
Lanzhou Jiaotong University (CN), Northwest Normal University (CN)
Openalex Percentile: Top 94%
Catalytic Alkyne Reactions
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