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1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis

Zurro, Mercedes and Mancheño, Olga García (2016) 1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis. The Chemical Record 17 (5), pp. 485-498.

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Other URL: http://doi.org/10.1002/tcr.201600104


Abstract

1,2,3-Triazoles are unique heterocycles with intriguing physical properties that allow not only the coordination to metals, but also the establishment of supramolecular interactions based on their polarized C-H bonds. In this account, an extensive work of our group on the design and application of 1,2,3-triazole catalysts is covered. Initially, a family of BINOL triazoles (Click-BINOLs) was ...

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Item type:Article
Date:2016
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Arbeitskreis Prof. Dr. Olga Garcia Mancheño
Identification Number:
ValueType
10.1002/tcr.201600104DOI
Keywords:ANION-BINDING CATALYSIS; REISSERT-TYPE REACTION; N-ACYLIMINIUM IONS; ENANTIOSELECTIVE ADDITION; ASYMMETRIC CATALYSIS; TERMINAL ALKYNES; CLICK CHEMISTRY; NUCLEOPHILIC DEAROMATIZATION; 1,3-DIPOLAR CYCLOADDITIONS; BIFUNCTIONAL CATALYST; Triazoles; Lewis Acid Catalysis; Anion-Binding Organocatalysis; Heterocycles; Dearomatization
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:39012
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