Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marino, Börjesson"'
Publikováno v:
Journal of the American Chemical Society. 143:20064-20070
Polysubstituted arenes are ubiquitous structures in a myriad of medicinal agents and complex molecules. Herein, we report a new catalytic blueprint that merges the modularity of nickel catalysis for bond formation with the ability to enable a rather
Autor:
Marino Börjesson, Xue-Qiang Wang, Ruben Martin, Basudev Sahoo, Yaya Duan, Daniel Janssen-Müller
Publikováno v:
Journal of the American Chemical Society. 142:16234-16239
A remote catalytic reductive sp2 C–H carboxylation of arenes with CO2 (1 bar) via 1,4-Ni migration is disclosed. This protocol constitutes the first catalytic 1,4-Ni migration reported to date, thu...
Autor:
Yuli, He, Marino, Börjesson, Huayue, Song, Yuhang, Xue, Daning, Zeng, Ruben, Martin, Shaolin, Zhu
Publikováno v:
Journal of the American Chemical Society. 143(48)
Polysubstituted arenes are ubiquitous structures in a myriad of medicinal agents and complex molecules. Herein, we report a new catalytic blueprint that merges the modularity of nickel catalysis for bond formation with the ability to enable a rather
Publikováno v:
Accounts of chemical research. 54(20)
The ubiquity and importance of carboxylic acids and amides in peptides, pharmaceuticals, agrochemicals, and synthetic materials has challenged chemists to design de novo catalytic carboxylation and amidation protocols. They represent a powerful alter
Autor:
Marino, Börjesson, Daniel, Janssen-Müller, Basudev, Sahoo, Yaya, Duan, Xueqiang, Wang, Ruben, Martin
Publikováno v:
Journal of the American Chemical Society. 142(38)
A remote catalytic reductive sp
Publikováno v:
Angewandte Chemie. 130:16178-16214
Publikováno v:
Chem. 5:254-256
Nitrogen-containing heterocycles are among the most ubiquitous motifs in pharmaceuticals. Therefore, the design of mild, practical, and modular protocols for their synthesis is still in high demand. In this issue of Chem, Molander and co-workers repo
Autor:
Keisho Okura, Marino Börjesson, Manuel van Gemmeren, Ruben Martin, Shang-Zheng Sun, Andreu Tortajada
Publikováno v:
Angewandte Chemie International Edition. 56:6558-6562
A switchable site-selective catalytic carboxylation of allylic alcohols has been developed in which CO2 is used with dual roles, both facilitating C-OH cleavage and as a C1 source. This protocol is characterized by its mild reaction conditions, absen
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
ACS Catalysis
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
ACS Catalysis
Recercat. Dipósit de la Recerca de Catalunya
instname
The recent years have witnessed the development of metal-catalyzed reductive carboxylation of organic (pseudo)halides with CO2 as C1 source, representing potential powerful alternatives to existing methodologies for preparing carboxylic acids, privil
Publikováno v:
Journal of the American Chemical Society. 138:7504-7507
A catalytic carboxylation of unactivated primary, secondary, and tertiary alkyl chlorides with CO2 at atmospheric pressure is described. This protocol represents the first intermolecular cross-electrophile coupling of unactivated alkyl chlorides, thu