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Article Dans Une Revue Synthesis: Journal of Synthetic Organic Chemistry Année : 2016

Synthesis of Heterobiaryls Featuring 1,4 N···S Inter-Ring Interactions

Résumé

Because of its low-lying σ* orbitals, the C-S bond can interact with electron donors. In this short review, our goal is to focus on intramol. interactions between bivalent sulfur and basic nitrogen atoms. In particular, we will consider the synthesis of selected heterobiaryls for which 1,4 N···S inter-ring interactions can be identified from X-ray diffraction data. Finally, we will briefly touch on the use of such conformational preferences in various applications. 1 Introduction 2 Cross-Coupling with C-C Bond Formation 3 Cross-Coupling with C-N Bond Formation 4 Nucleophilic Addn. to Azine Followed by Oxidn. 5 Multicomponent Reactions 6 Heterobiaryl Formation by Azine Building 7 Heterobiaryl Formation by Building of the Sulfur-Contg. Heterocycle 8 Cycloaddn. Reactions 9 Other Syntheses 10 Conclusion.
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Dates et versions

hal-01231159 , version 1 (28-06-2022)

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David Tilly, Floris Chevallier, Florence Mongin. Synthesis of Heterobiaryls Featuring 1,4 N···S Inter-Ring Interactions. Synthesis: Journal of Synthetic Organic Chemistry, 2016, 48 (02), pp.184-199. ⟨10.1055/s-0035-1560360⟩. ⟨hal-01231159⟩
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