Stereoselective Synthesis of Benzosultam-Fused Tetrahydroquinazolines via [4+2]-Cycloaddition of Cyclic N-Sulfonyl Ketimines with 2-Aminophenyl Enones

Abstract A [4+2]-cycloaddition reaction between cyclic N-sulfonyl ketimines and 2-aminophenyl enones, catalyzed by K2CO3, has been developed. This method provides a straightforward and efficient approach for synthesizing a wide range of structurally complex and highly functionalized benzosultam-fused tetrahydroquinazolines in high yields, with excellent diastereoselectivities.

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Publication Details

Journal
Synthesis
Published
2025-03-26
DOI
https://doi.org/10.1055/a-2567-4696
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Stereoselective Synthesis of Benzosultam-Fused Tetrahydroquinazolines via [4+2]-Cycloaddition of Cyclic N-Sulfonyl Ketimines with 2-Aminophenyl Enones

Sung‐Gon Kim, Ji Won Han
Synthesis
Quinazolinone synthesis and applications
article

Stereoselective Synthesis of Benzosultam-Fused Tetrahydroquinazolines via [4+2]-Cycloaddition of Cyclic N-Sulfonyl Ketimines with 2-Aminophenyl Enones

Sung‐Gon Kim, Ji Won Han
article en

Abstract

Abstract A [4+2]-cycloaddition reaction between cyclic N-sulfonyl ketimines and 2-aminophenyl enones, catalyzed by K2CO3, has been developed. This method provides a straightforward and efficient approach for synthesizing a wide range of structurally complex and highly functionalized benzosultam-fused tetrahydroquinazolines in high yields, with excellent diastereoselectivities.

SynthesisVol. 57(13)
Kyonggi University (KR)
National Research Foundation of Korea
Openalex Percentile: Top 96%
Quinazolinone synthesis and applications
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