Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Michael E. Muratore"'
Publikováno v:
Expert opinion on therapeutic patents. 32(5)
INTRODUCTION : Ubiquitin specific peptidase 30 (USP30) is a mitochondrial deubiquitinase that antagonizes ubiquitination-mediated mitophagy of damaged or impaired mitochondria driven by the activity of PARK2/Parkin ubiquitin ligase and PINK1 protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7accdc675fe10946451e06d3bf1656f6
https://pubmed.ncbi.nlm.nih.gov/34743664
https://pubmed.ncbi.nlm.nih.gov/34743664
Autor:
Rodrigo Ramírez‐Contreras, Marc Montesinos-Magraner, Michael E. Muratore, Abraham Mendoza, Magnus Johansson, Matteo Costantini
Publikováno v:
Angewandte Chemie International Edition
Asymmetric cyclopropane synthesis currently requires bespoke strategies, methods, substrates, and reagents, even when targeting similar compounds. This approach slows down discovery and limits available chemical space. Introduced herein is a practica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f3415ff3882eb0da6f1304f24c7abb1
https://doi.org/10.1002/anie.201814123
https://doi.org/10.1002/anie.201814123
Autor:
Xichen Lin, Michael E. Muratore, Huijie Li, Ami S. Lakdawala, Jakob Busch-Petersen, Ruth R. Osborn, David D. Miller, Jeffrey K. Kerns, Rick P. C. Cousins, Ian Robert Baldwin, Paul Bamborough, John Yonchuk, Ann M. Bullion, Lin Guoliang, Jeffrey C. Boehm, Wei Fu, John A. Christopher, Edward F. Webb, Roderick S. Davis, William L. Rumsey, Rita Field, Jeremy John Payne, Hong Nie
Publikováno v:
ACS Medicinal Chemistry Letters. 9:1164-1169
[Image: see text] IκB kinase β (IKKβ or IKK2) is a key regulator of nuclear factor kappa B (NF-κB) and has received attention as a therapeutic target. Herein we report on the optimization of a series of 3,5-disubstituted-indole-7-carboxamides for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::782cb7b7a63c400db0be5e5461917822
https://doi.org/10.1021/acsmedchemlett.8b00291
https://doi.org/10.1021/acsmedchemlett.8b00291
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
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Recercat. Dipósit de la Recerca de Catalunya
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The reaction of oxime-tethered 1,6-enynes with a cationic gold(I) catalyst demonstrates a great potential for the synthesis of a range of heterocycles in a diastereospecific fashion. The control of the configuration of the oxime and the alkene of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e491c4453f85c5e426e4c46281b448a9
https://doi.org/10.1002/chem.201802770
https://doi.org/10.1002/chem.201802770
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 140(16), 5393-5400
RECERCAT (Dipòsit de la Recerca de Catalunya)
Journal of the American Chemical Society 140 (2018) 16
Recercat. Dipósit de la Recerca de Catalunya
instname
Journal of the American Chemical Society, 140(16), 5393-5400
RECERCAT (Dipòsit de la Recerca de Catalunya)
Journal of the American Chemical Society 140 (2018) 16
Recercat. Dipósit de la Recerca de Catalunya
instname
The total synthesis of seven members of the lapidilectine and grandilodine family of alkaloids has been accomplished in racemic and enantiopure form without protection/deprotection of functional groups. The two key steps, an 8-endo-dig hydroarylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83cb40ecab4c070857121251ec4bd63e
http://europepmc.org/articles/PMC5920919
http://europepmc.org/articles/PMC5920919
Autor:
Laurent Evanno, Mariia S. Kirillova, Fanny Roussi, Gaëla Cauchie, Pierre Champy, Marc Litaudon, Guy Lewin, Anne-Marie Le Ray, Raphaël Grougnet, Erwan Poupon, Marina Kritsanida, Lengo Mambu, Alexander E. Fox Ramos, Antonio M. Echavarren, Fedor M. Miloserdov, Pascal Richomme-Peniguel, Michel Frederich, Khalijah Awang, Sylvie Michel, Hazrina Hazni, Dimitri Bréard, Pierre Le Pogam, Christelle Lémus, Marion Girardot, Elvis Otogo N’Nang, Michael E. Muratore, Mehdi A. Beniddir, Charlotte Fox Alcover, Thomas Gaslonde
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Scientific Data, Vol 6, Iss 1, Pp 1-6 (2019)
Scientific Data
Scientific Data, Nature Publishing Group, 2019, 6 (15), pp.1-6. ⟨10.1038/s41597-019-0028-3⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Scientific Data 6 (2019) 1
Scientific Data, 2019, 6 (15), pp.1-6. ⟨10.1038/s41597-019-0028-3⟩
Scientific Data, 6(1)
Scientific Data, Vol 6, Iss 1, Pp 1-6 (2019)
Scientific Data
Scientific Data, Nature Publishing Group, 2019, 6 (15), pp.1-6. ⟨10.1038/s41597-019-0028-3⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Scientific Data 6 (2019) 1
Scientific Data, 2019, 6 (15), pp.1-6. ⟨10.1038/s41597-019-0028-3⟩
Scientific Data, 6(1)
This Data Descriptor announces the submission to public repositories of the monoterpene indole alkaloid database (MIADB), a cumulative collection of 172 tandem mass spectrometry (MS/MS) spectra from multiple research projects conducted in eight natur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7a00dcd0e298fcf9266c3af8571bad
https://doi.org/10.1038/s41597-019-0028-3
https://doi.org/10.1038/s41597-019-0028-3
Autor:
Christian Sköld, Michael E. Muratore, Ina Terstiege, Anna Tomberg, Magnus Johansson, Per-Ola Norrby
Publikováno v:
iScience, Vol 20, Iss, Pp 373-391 (2019)
iScience
iScience
Summary Efficient functionalization of C−H bonds can be achieved using transition metal catalysts, such as Pd(OAc)2. To better control the regioselectivity in these reactions, some functional groups on the substrate may be used as directing groups,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bf520cd770edbdc47a2c1bf226cf29f
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-397315
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-397315
Autor:
Magnus Johansson, Michael E. Muratore, Matteo Costantini, Marc Montesinos-Magraner, Rodrigo Ramírez‐Contreras, Abraham Mendoza
Publikováno v:
ChemRxiv
Asymmetric cyclopropane synthesis currently requires bespoke strategies, methods, substrates and reagents, even when targeting similar compounds. This limits the speed and chemical space available for discovery campaigns. Here we introduce a practica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be78a977396468ebc9c52731a7707ab
https://doi.org/10.26434/chemrxiv.7436795.v1
https://doi.org/10.26434/chemrxiv.7436795.v1
Autor:
Michael E. Muratore, Francesco Camponovo, Morgane Gaydou, Antonio M. Echavarren, Javier Carreras, Ricarda E. Miller
Publikováno v:
The Journal of Organic Chemistry
A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF6 as a general purpose catalyst. The resulting adducts can be easily converted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0e2466f86973d5fc1b2a85383118438
https://doi.org/10.1021/acs.joc.5b02607
https://doi.org/10.1021/acs.joc.5b02607
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Chemistry-A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositori Institucional de la Universitat Rovira i Virgili
Consejo Superior de Investigaciones Científicas (CSIC)
Chemistry-A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositori Institucional de la Universitat Rovira i Virgili
Consejo Superior de Investigaciones Científicas (CSIC)
By reviewing the recent progress on the elucidation of the structure of gold carbenes and the definitions of metal carbenes and carbenoids, we recommend to use the term gold carbene to describe gold carbene-like intermediates, regardless of whether t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::025ac2cbc058c65815e6b4d52654aef0
https://doi.org/10.1002/chem.201406318
https://doi.org/10.1002/chem.201406318