Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gadde Sathish Kumar"'
Autor:
Rajesh Kancherla, Krishnamoorthy Muralirajan, Bholanath Maity, Safakath Karuthedath, Gadde Sathish Kumar, Frédéric Laquai, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
Although the combination of photo- and nickel catalysis has garnered intense interest in the preceding years, the mechanisms by which these transformations occur are to some degree unresolved. Here the authors provide computational and spectroscopic
Externí odkaz:
https://doaj.org/article/cd49c2633c5543fa87a7adaa24234737
Autor:
Jose J. Delgado-Marín, Alejandra Rendón-Patiño, Vijay Kumar Velisoju, Gadde Sathish Kumar, Naydu Zambrano, Magnus Rueping, Jorge Gascón, Pedro Castaño, Javier Narciso, Enrique V. Ramos-Fernandez
Zeolitic imidazolate frameworks (ZIFs) have been profusely used as catalysts for inserting CO2 into organic epoxides (i.e., epichlorohydrin) through cycloaddition. Here, we demonstrate that these materials suffer from irreversible degradation by leac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dccaf5ad63613fbdfe237c956670f8a
https://hdl.handle.net/10045/130870
https://hdl.handle.net/10045/130870
Autor:
Gadde Sathish Kumar, Prashant S. Shinde, Haifeng Chen, Krishnamoorthy Muralirajan, Rajesh Kancherla, Magnus Rueping
Publikováno v:
Organic letters. 24(35)
A decarboxylative cyanation of amino acids under paired electrochemical reaction conditions has been developed. 4-CN-pyridine was found to be a new and effective cyanation reagent under catalyst-free conditions. Mechanistic studies support a nucleoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bb95f30ec10c5008ebbaa2589364da0
https://pubmed.ncbi.nlm.nih.gov/36036921
https://pubmed.ncbi.nlm.nih.gov/36036921
Autor:
Rajesh Kancherla, Krishnamoorthy Muralirajan, Bholanath Maity, Safakath Karuthedath, Gadde Sathish Kumar, Frédéric Laquai, Luigi Cavallo, Magnus Rueping
Publikováno v:
Nature communications. 13(1)
Various methods that use a photocatalyst for electron transfer between an organic substrate and a transition metal catalyst have been established. While triplet sensitization of organic substrates via energy transfer from photocatalysts has been demo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa9f64e2020a8cd76ec6fa0be18a9e7
https://pubmed.ncbi.nlm.nih.gov/35585041
https://pubmed.ncbi.nlm.nih.gov/35585041
Autor:
Gadde Sathish Kumar, Pavlo Nikolaienko, Aleksandra Brzozowska, Magnus Rueping, Chen Zhu, Anatoly A. Peshkov
Publikováno v:
Angewandte Chemie (International ed. in English). 59(16)
The first electrochemical approach for nickel-catalyzed cross-electrophile coupling was developed. This method provides a novel route to 1,1-diarylalkane derivatives from simple and readily available alkyl and aryl halides in good yields and excellen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd793741e6d84afa82fa4a14459ef3a
https://pubmed.ncbi.nlm.nih.gov/32017340
https://pubmed.ncbi.nlm.nih.gov/32017340
Autor:
Kallu Rajender Reddy, Gadde Sathish Kumar, Pailla Santhosh Kumar, M. Lakshmi Kantam, Nagireddy Veera Reddy
Publikováno v:
Synlett. 25:2133-2138
An oxidative approach for the synthesis of phenyl carbamates has been achieved by ligand-assisted copper-catalyzed cross-dehydrogenative coupling (CDC) of phenols with formamides. The direct coupling of simple phenols with mono- and dialkyl formami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a52df11038b45aae8145b827f0cb2cbd
https://doi.org/10.1055/s-0034-1378519
https://doi.org/10.1055/s-0034-1378519
Publikováno v:
ChemInform. 47
A synthetic method to prepare (E)-(pyridin-2-yl)enones and (E)-(quinolin-8-yl)enones that relies on the respective copper(I)-catalyzed formal cross-dehydrogenative coupling (CDC) reaction of 2-methylpyridine and 8-methylquinoline with methyl ketones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af21046476cbbfe54b325982f6d82ed
https://doi.org/10.1002/chin.201625163
https://doi.org/10.1002/chin.201625163
Publikováno v:
Chemistry, an Asian journal. 11(3)
A synthetic method to prepare (E)-(pyridin-2-yl)enones and (E)-(quinolin-8-yl)enones that relies on the respective copper(I)-catalyzed formal cross-dehydrogenative coupling (CDC) reaction of 2-methylpyridine and 8-methylquinoline with methyl ketones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f848138ede37da4763cbce0e538237
https://pubmed.ncbi.nlm.nih.gov/26586026
https://pubmed.ncbi.nlm.nih.gov/26586026
Autor:
Nagireddy Veera Reddy, M. Lakshmi Kantam, Kallu Rajender Reddy, Pailla Santhosh Kumar, Gadde Sathish Kumar
Publikováno v:
ChemInform. 46
An oxidative approach for the synthesis of phenyl carbamates has been achieved by ligand-assisted copper-catalyzed cross-dehydrogenative coupling (CDC) of phenols with formamides. The direct coupling of simple phenols with mono- and dialkyl formami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9207ca30709ee392338a3c004faae62a
https://doi.org/10.1002/chin.201509104
https://doi.org/10.1002/chin.201509104