Abstract
A series of chiral N-heterocyclic carbene precursors based on the dihydroimidazole framework were prepared from easily available chiral amines. The sequential attachment of these amines and mesitylamine to chloroacetyl chloride followed by reduction and subsequent ring closure gave the desired dihydroimidazolium salts in good yield.
Keywords: Heterocyclic carbenes, chirality, chiral amines, ring closure, imidazolium salts
Letters in Organic Chemistry
Title: The Modular Synthesis of Chiral N-Heterocyclic Carbene Precursors
Volume: 4 Issue: 8
Author(s): Attila Paczal and Andras Kotschy
Affiliation:
Keywords: Heterocyclic carbenes, chirality, chiral amines, ring closure, imidazolium salts
Abstract: A series of chiral N-heterocyclic carbene precursors based on the dihydroimidazole framework were prepared from easily available chiral amines. The sequential attachment of these amines and mesitylamine to chloroacetyl chloride followed by reduction and subsequent ring closure gave the desired dihydroimidazolium salts in good yield.
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Cite this article as:
Paczal Attila and Kotschy Andras, The Modular Synthesis of Chiral N-Heterocyclic Carbene Precursors, Letters in Organic Chemistry 2007; 4 (8) . https://dx.doi.org/10.2174/157017807782795565
DOI https://dx.doi.org/10.2174/157017807782795565 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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