Publication:
Spontaneous macrocyclization through multiple dynamic cyclic aminal formation.

dc.contributor.authorCarbajo, Daniel
dc.contributor.authorRuiz-Sánchez, Antonio Jesús
dc.contributor.authorNájera, Francisco
dc.contributor.authorPérez-Inestrosa, Ezequiel
dc.contributor.authorAlfonso, Ignacio
dc.date.accessioned2023-02-09T10:39:45Z
dc.date.available2023-02-09T10:39:45Z
dc.date.issued2021
dc.description.abstractThe use of aminals in dynamic covalent chemistry is slightly underexplored, probably due to their inherent instability. Here we report the spontaneous [2+2] macrocyclization of tetrakis(aminals). Their unexpected stability and structural modularity, the dynamic nature of the connections and their water tolerance make them appealing systems for future applications as stimulus-responsive materials.
dc.identifier.doi10.1039/d0cc07184f
dc.identifier.essn1364-548X
dc.identifier.pmid33448267
dc.identifier.unpaywallURLhttps://pubs.rsc.org/en/content/articlepdf/2021/cc/d0cc07184f
dc.identifier.urihttp://hdl.handle.net/10668/16982
dc.issue.number10
dc.journal.titleChemical communications (Cambridge, England)
dc.journal.titleabbreviationChem Commun (Camb)
dc.language.isoen
dc.organizationCentro Andaluz de Nanomedicina y Biotecnología-BIONAND
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.page.number1190-1193
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.titleSpontaneous macrocyclization through multiple dynamic cyclic aminal formation.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number57
dspace.entity.typePublication

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