ArticleOrganic letters2016
Synthesis of Cyclic Guanidines via Silver-Catalyzed Intramolecular Alkene Hydroamination Reactions of N-Allylguanidines.
Article in Organic letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Silver acetate-catalyzed synthesis of cyclic sulfonyl guanidine with exocyclic double bond.Molecular diversity · 2023Article
- Prediction of explosive properties of newly synthesized amino nitroguanidine-based energetic complexes via density functional theory.Journal of molecular modeling · 2020Article
- Divergent 2-Chloroquinazolin-4(3H)-one Rearrangement: Twisted-Cyclic Guanidine Formation or Ring-Fused N-Acylguanidines via a Domino Process.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
- Generation and Reactivity of 2-Amido-1,3-diaminoallyl Cations: Cyclic Guanidine Annulations via Net (3 + 2) and (4 + 3) Cycloadditions.Organic letters · 2020Article
- Synthesis of Cyclic Guanidines Bearing N-Arylsulfonyl and N-Cyano Protecting Groups via Pd-Catalyzed Alkene Carboamination Reactions.Organic letters · 2017Article
- An Expeditious and Greener Synthesis of 2-Aminoimidazoles in Deep Eutectic Solvents.Molecules (Basel, Switzerland) · 2016Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The silver-catalyzed hydroamination of tosyl-protected N-allylguanidines is described. These reactions provide substituted cyclic guanidines in high yields. The reactions are amenable to the construction of quaternary stereocenters as well as both monocyclic and bicyclic guanidine products.
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Registered trials
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