Chemo-, regio-, and stereoselective heterocyclization of sulfonamides and <scp>d</scp>-limonene with solvent interception

A method for chemo-, regio- and stereoselective assembling of 3 a ,4,5,6,7,7 a -hexahydro-1 H -benzo[ d ]imidazoles from arenesulfonamides and d -limonene with NBS in acetonitrile in up to 87% yield is proposed.

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Publication Details

Journal
New Journal of Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5nj02510a
Primary Topic
Chemical synthesis and alkaloids
Type
article
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article

Chemo-, regio-, and stereoselective heterocyclization of sulfonamides and d-limonene with solvent interception

Mikhail Yu. Moskalik, S. V. Zinchenko, Bagrat А. Shainyan, Vera V. Astakhova et al.
New Journal of Chemistry
Chemical synthesis and alkaloids
article

Chemo-, regio-, and stereoselective heterocyclization of sulfonamides and d-limonene with solvent interception

Mikhail Yu. Moskalik, S. V. Zinchenko, Bagrat А. Shainyan, Vera V. Astakhova, Tatyana N. Borodina, Valentina S. Myasnikova
article en

Abstract

A method for chemo-, regio- and stereoselective assembling of 3 a ,4,5,6,7,7 a -hexahydro-1 H -benzo[ d ]imidazoles from arenesulfonamides and d -limonene with NBS in acetonitrile in up to 87% yield is proposed.

New Journal of ChemistryVol. 49(41)
A.E. Favorsky Irkutsk Institute of Chemistry (RU)
Openalex Percentile: Top 79%
Chemical synthesis and alkaloids
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