Synthesis of chiral cyclohexane-linked bisimidazolines

Both chiral bisoxazolines and bisimidazolines are efficient chiral ligands in metal-catalyzed asymmetric organic transformations. Chiral cyclohexane-linked bisimidazolines were prepared from optically active cyclohexane-1,2-dicarboxylic acid and 1,2-diphenylethane-1,2-diamines via the monosulfonylation of 1,2-diphenylethane-1,2-diamines, condensation of <i>N</i>-sulfonylated 1,2-diphenylethane-1,2-diamines and cyclohexane-1,2-dicarboxylic acid, and the final cyclization with the in situ generated Hendrickson reagent.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2025-09-04
DOI
https://doi.org/10.3762/bjoc.21.140
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of chiral cyclohexane-linked bisimidazolines

Changmeng Xi, Qi Sun, Jiaxi Xu
Beilstein Journal of Organic Chemistry
Synthesis and Catalytic Reactions
article

Synthesis of chiral cyclohexane-linked bisimidazolines

Changmeng Xi, Qi Sun, Jiaxi Xu
article en

Abstract

Both chiral bisoxazolines and bisimidazolines are efficient chiral ligands in metal-catalyzed asymmetric organic transformations. Chiral cyclohexane-linked bisimidazolines were prepared from optically active cyclohexane-1,2-dicarboxylic acid and 1,2-diphenylethane-1,2-diamines via the monosulfonylation of 1,2-diphenylethane-1,2-diamines, condensation of <i>N</i>-sulfonylated 1,2-diphenylethane-1,2-diamines and cyclohexane-1,2-dicarboxylic acid, and the final cyclization with the in situ generated Hendrickson reagent.

Beilstein Journal of Organic ChemistryVol. 21
Beijing University of Chemical Technology (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 82%
Synthesis and Catalytic Reactions
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