Diastereoselective synthesis of 1,4-diaryl piperazines through the dimerization of 3-aminooxetanes with cooperative indium–diphenyl phosphate catalysis

A catalytic dimerization reaction of 3-aminooxetanes has been developed with cooperative indium/diphenyl phosphate catalysis, successfully achieving a [3 + 3] annulation reaction to provide a series of piperazine derivatives. The reaction features good functional group compatibility and excellent diastereoselectivity, enabling the synthesis of the corresponding piperazine products in moderate to good yields. The hydroxymethyl group present in the products could serve as a privileged moiety for diverse transformations, permitting the further elaboration of piperazine-based molecules.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc03616j
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Diastereoselective synthesis of 1,4-diaryl piperazines through the dimerization of 3-aminooxetanes with cooperative indium–diphenyl phosphate catalysis

Jianwei Sun, Hai Huang, Zhengyu Han, Cuicui Nian et al.
1 citations
Chemical Communications
Synthesis and Catalytic Reactions
0.94
article

Diastereoselective synthesis of 1,4-diaryl piperazines through the dimerization of 3-aminooxetanes with cooperative indium–diphenyl phosphate catalysis

Jianwei Sun, Hai Huang, Zhengyu Han, Cuicui Nian, Long Cheng
article en
1 citations

Abstract

A catalytic dimerization reaction of 3-aminooxetanes has been developed with cooperative indium/diphenyl phosphate catalysis, successfully achieving a [3 + 3] annulation reaction to provide a series of piperazine derivatives. The reaction features good functional group compatibility and excellent diastereoselectivity, enabling the synthesis of the corresponding piperazine products in moderate to good yields. The hydroxymethyl group present in the products could serve as a privileged moiety for diverse transformations, permitting the further elaboration of piperazine-based molecules.

Chemical CommunicationsVol. 61(71)
Hong Kong University of Science and Technology (HK), Changzhou University (CN)
Openalex Percentile: Top 23%
Synthesis and Catalytic Reactions
0.94
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