Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Julia Bamberger"'
Autor:
Julia Bamberger, Florian Ostler, Olga García Mancheño, Pascal Steinforth, Dariusz G. Piekarski, Monika Schönhoff, Melania Gómez‐Martínez
Publikováno v:
Chemistry – A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry (Weinheim an Der Bergstrasse, Germany)
H‐bond donor catalysts able to modulate the reactivity of ionic substrates for asymmetric reactions have gained great attention in the past years, leading to the development of cooperative multidentate H‐bonding supramolecular structures. However
Publikováno v:
ChemCatChem
Chemcatchem
Chemcatchem
Non‐covalent molecular interactions on the basis of halogen and chalcogen bonding represent a promising, powerful catalytic activation mode. However, these “unusual” non‐covalent interactions are typically employed in the solid state and scar
Autor:
Dariusz G. Piekarski, Pascal Steinforth, Melania Gómez-Martínez, Julia Bamberger, Florian Ostler, Monika Schönhoff, Olga Garcia Mancheño
Herein, insights into the cooperativity nature, anion binding strength, and folding mechanism of a model chiral triazole catalyst is presented. Our combined experimental and computational study revealed that multi-interaction catalysts exhibiting wea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::f02655d3b5381134a83eaf1b31dcd7c0
https://zenodo.org/record/4073078
https://zenodo.org/record/4073078
Autor:
Julia Bamberger, Dariusz G. Piekarski, Olga García Mancheño, Melania Gómez‐Martínez, Theresa Fischer
Publikováno v:
Angewandte Chemie
Autor:
Andrea Gini, Rubén Mas-Ballesté, Mercedes Zurro, Julia Bamberger, José Alemán, Olga García Mancheño, Javier Luis-Barrera
Publikováno v:
ResearcherID
A metal-free synthesis of biologically important benzazepines is achieved through a single synthetic operation involving an oxidative C–H bond functionalization and ring expansion with diazomethanes as key reagent. This represents a new, strong met
Publikováno v:
Chemistry - A European Journal. 22:3785-3793
Easily accessible and tunable chiral triazoles have been introduced as a novel class of C-H bond-based H-donors for anion-binding organocatalysis. They have proven to be effective catalysts for the dearomatization reaction of different N-heteroarenes
Publikováno v:
ChemInform. 47
Easily accessible and tunable chiral triazoles have been introduced as a novel class of C-H bond-based H-donors for anion-binding organocatalysis. They have proven to be effective catalysts for the dearomatization reaction of different N-heteroarenes
Publikováno v:
Organicbiomolecular chemistry. 14(24)
The first anion-binding organocatalyzed enantioselective Reissert-type dearomatization of diazarenes has been developed. This reaction represents a synthetic challenge since diazarenes have various reactive sites. The use of a chiral tetrakistriazole
Autor:
Theresa Fischer, Julia Bamberger, Olga García Mancheño, Dariusz G. Piekarski, Melania Gómez‐Martínez
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
A general and highly enantioselective synthesis of oxygen heterocycles from readily available in situ generated pyrylium derivatives has been realized by embracing a multi‐coordination approach with helical anion‐binding tetrakistriazole catalyst