JOURNAL ARTICLE

Expanded‐Ring and Backbone‐Functionalised N‐Heterocyclic Carbenes

Abstract

Abstract An unsaturated seven‐membered amidinium salt 7 decomposes in the presence of metal salts under basic conditions. However, 7 readily forms a Diels–Alder cycloadduct with CpH from which the Rh I complexes may be prepared. Thus, structurally elaborate, sterically crowded carbene ligand complexes bearing peripheral unsaturated functionality are available in a short versatile synthesis.

Keywords:
Chemistry Carbene Steric effects Salt (chemistry) Ring (chemistry) Ligand (biochemistry) Combinatorial chemistry Stereochemistry Organic chemistry Catalysis Receptor

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27
Cited By
2.31
FWCI (Field Weighted Citation Impact)
38
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0.87
Citation Normalized Percentile
Is in top 1%
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Citation History

Topics

N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Physical Sciences →  Chemistry →  Organic Chemistry
Catalytic Cross-Coupling Reactions
Physical Sciences →  Chemistry →  Organic Chemistry
Synthetic Organic Chemistry Methods
Physical Sciences →  Chemistry →  Organic Chemistry

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