Relay Catalysis-EnabledEnantioselective Annulationsof β,γ-Alkynyl-α-imino Esters with 1,3-Diones forthe Divergent Synthesis of Chiral Oxacycles

A novel protocol for the chemically divergent synthesis of chiral oxacycles has been developed using organo/metal relay catalysis. The methodology integrates a stereospecific Mannich reaction between β,γ-alkynyl-α-imino esters and 1,3-diones catalyzed by a chiral bifunctional squaramide, followed by Lewis acid-catalyzed regioselective annulation reactions. By switching the Lewis acid employed, we achieved a divergent pathway to construct structurally related pyran and furan derivatives from a common intermediate. The (3+3) and (3+2) annulation products were obtained in high yields and excellent stereoselectivities. Comprehensive mechanistic studies were conducted to establish the reaction mechanism.

Publication Details

Journal
Figshare
Published
2025-02-19
DOI
https://doi.org/10.1021/acs.orglett.5c00233.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Relay Catalysis-EnabledEnantioselective Annulationsof β,γ-Alkynyl-α-imino Esters with 1,3-Diones forthe Divergent Synthesis of Chiral Oxacycles

Figshare
Catalytic C–H Functionalization Methods
article

Relay Catalysis-EnabledEnantioselective Annulationsof β,γ-Alkynyl-α-imino Esters with 1,3-Diones forthe Divergent Synthesis of Chiral Oxacycles

article en

Abstract

A novel protocol for the chemically divergent synthesis of chiral oxacycles has been developed using organo/metal relay catalysis. The methodology integrates a stereospecific Mannich reaction between β,γ-alkynyl-α-imino esters and 1,3-diones catalyzed by a chiral bifunctional squaramide, followed by Lewis acid-catalyzed regioselective annulation reactions. By switching the Lewis acid employed, we achieved a divergent pathway to construct structurally related pyran and furan derivatives from a common intermediate. The (3+3) and (3+2) annulation products were obtained in high yields and excellent stereoselectivities. Comprehensive mechanistic studies were conducted to establish the reaction mechanism.

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Openalex Percentile: Top 69%
Catalytic C–H Functionalization Methods
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