Organocatalytic Hat Trick: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD)-Catalyzed Synthesis of Cyclic Imides via an Amidation–Cyclization–Elimination Cascade

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) was used for the synthesis of cyclic imides via an amidation-cyclization-elimination cascade. This organocatalytic transformation features both the traditional reactivity of TBD and its unprecedented C-C bond cleavage capability, allowing rapid and efficient access to cyclic imides. This method is compatible with the late-stage functionalization of complex molecules and the synthesis of bioactive molecules. Both experimental and computational approaches were employed to gain a better understanding of the reaction mechanism.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-12-12
DOI
https://doi.org/10.1021/acs.joc.4c02649
Citations
2
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.47

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article

Organocatalytic Hat Trick: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD)-Catalyzed Synthesis of Cyclic Imides via an Amidation–Cyclization–Elimination Cascade

Karine Auclair, Chunling Blue Lan
2 citations
The Journal of Organic Chemistry
Chemical Synthesis and Analysis
0.47
article

Organocatalytic Hat Trick: 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD)-Catalyzed Synthesis of Cyclic Imides via an Amidation–Cyclization–Elimination Cascade

Karine Auclair, Chunling Blue Lan
article en
2 citations

Abstract

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) was used for the synthesis of cyclic imides via an amidation-cyclization-elimination cascade. This organocatalytic transformation features both the traditional reactivity of TBD and its unprecedented C-C bond cleavage capability, allowing rapid and efficient access to cyclic imides. This method is compatible with the late-stage functionalization of complex molecules and the synthesis of bioactive molecules. Both experimental and computational approaches were employed to gain a better understanding of the reaction mechanism.

The Journal of Organic ChemistryVol. 90(1)
McGill University (CA)
Canadian Institutes of Health Research, Fonds de recherche du Québec – Nature et technologies
Openalex Percentile: Top 34%
Chemical Synthesis and Analysis
0.47
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