Organic Transformations Utilizing 1,5,7‐Triazabicyclo[4.4.0]Dec‐5‐Ene (TBD): A Tale of Two Nitrogens

Abstract 1,5,7‐Triazabicyclo[4.4.0]dec‐5‐ene (TBD) is a bicyclic guanidine with booming applications. Bearing both a sp 2 ‐hybridized nitrogen and an adjacent N−H bond, TBD is a multifunctional and versatile reagent that is able to promote a variety of organic transformations. Although advancements with TBD in the polymer field have been well reviewed and documented, summaries that focus on synthetic methodologies are scarce. This review intends to provide a concise overview of synthetic methods utilizing TBD published over the past two decades. Classified based on the primary function of TBD, diverse transformations are described, and reaction mechanisms are incorporated when necessary. Examples from various fields are covered, including methodology developments, natural product syntheses, medicinal chemistry applications, as well as industrial utilizations.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-02-03
DOI
https://doi.org/10.1002/ejoc.202401383
Citations
6
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
4.74
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article

Organic Transformations Utilizing 1,5,7‐Triazabicyclo[4.4.0]Dec‐5‐Ene (TBD): A Tale of Two Nitrogens

Karine Auclair, Chunling Blue Lan
6 citations
European Journal of Organic Chemistry
Chemical Reactions and Isotopes
4.74
article

Organic Transformations Utilizing 1,5,7‐Triazabicyclo[4.4.0]Dec‐5‐Ene (TBD): A Tale of Two Nitrogens

Karine Auclair, Chunling Blue Lan
article en
6 citations

Abstract

Abstract 1,5,7‐Triazabicyclo[4.4.0]dec‐5‐ene (TBD) is a bicyclic guanidine with booming applications. Bearing both a sp 2 ‐hybridized nitrogen and an adjacent N−H bond, TBD is a multifunctional and versatile reagent that is able to promote a variety of organic transformations. Although advancements with TBD in the polymer field have been well reviewed and documented, summaries that focus on synthetic methodologies are scarce. This review intends to provide a concise overview of synthetic methods utilizing TBD published over the past two decades. Classified based on the primary function of TBD, diverse transformations are described, and reaction mechanisms are incorporated when necessary. Examples from various fields are covered, including methodology developments, natural product syntheses, medicinal chemistry applications, as well as industrial utilizations.

European Journal of Organic ChemistryVol. 28(12)
McGill University (CA)
Openalex Percentile: Top 6%
Chemical Reactions and Isotopes
4.74
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