Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Carbamoyl chloride"'
Publikováno v:
Surgical Case Reports, Vol 9, Iss 1, Pp 1-4 (2023)
Abstract Background Necrotizing fasciitis in neonates is a rare and life-threatening infection involving necrosis of the skin, subcutaneous tissues, deep fascia, and sometimes underlying muscles, with a fulminant course and high mortality rate. Necro
Externí odkaz:
https://doaj.org/article/bb3df23a715d4864bfc7b703c7b651d9
Publikováno v:
Brazilian Archives of Biology and Technology, Vol 58, Iss 3, Pp 431-442 (2015)
This work studied the synthesis of 5,10,15-tris(4-aminophenyl)-20-(N,N-dialkyl/diaryl-N-phenylurea) porphyrins (P1-P4 with alkyl or aryl groups of Ph, iPr, Et and Me, respectively) and also the preparation of their manganese (III) and cobalt (II) com
Externí odkaz:
https://doaj.org/article/236a766b8cec446c98e04aeafad01a79
Publikováno v:
Synlett. 32:955-961
Chiral-auxiliary-mediated synthesis represents the most frequently used synthetic tool for the induction of chirality on α-position of γ-lactams in organic synthesis. However, the general strategy requires the stoichiometric use of chiral reagents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d54fac8ca47bec6fbdb9afa0694697e
https://doi.org/10.1055/a-1353-7605
https://doi.org/10.1055/a-1353-7605
Publikováno v:
Journal of the American Chemical Society. 142:15654-15660
Herein, we report a nickel-catalyzed reductive cross-coupling reaction of easily accessible 3-butenyl carbamoyl chloride with primary alkyl iodide to access the chiral α-alkylated pyrrolidinone with broad substrate scope and high enantiomeric excess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4378dcb26cf6f4c2aba028b99ab8215
https://doi.org/10.1021/jacs.0c07126
https://doi.org/10.1021/jacs.0c07126
Publikováno v:
Organic Letters. 22:6376-6381
Reported herein is a palladium/copper cooperative-catalyzed dicarbofunctionalization of alkene-tethered carbamoyl chlorides with 1,1-diborylmethane. This cyclization/deborylation cascade strategy allows for the expedient formation of the versatile bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c05e3cfd133bef270ce48fa19163a57e
https://doi.org/10.1021/acs.orglett.0c02211
https://doi.org/10.1021/acs.orglett.0c02211
Akademický článek
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Autor:
Paula de Souza Silva Freitas, Lucas Dalvi Armond Rezende, Kelly Eduarda de Jesus Silva, Bruno Henrique Fiorin, Ramon Araújo dos Santos, Aline de Oliveira Ramalho
Publikováno v:
Estima, Vol 19 (2021)
Objectives: The aim was to identify the benefits of using Dialkyl Carbamoyl Chloride for the treatment of biofilms in wounds. Methods: This is an integrative literature review that aimed to answer the guiding question: “What are the benefits of usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede6031579dcdc3b45a48f66be4f987e
https://doi.org/10.30886/estima.v19.1087_in
https://doi.org/10.30886/estima.v19.1087_in
Autor:
Egor M. Larin, Mark Lautens
Publikováno v:
Angewandte Chemie International Edition. 58:13438-13442
Acyl substituted triazoles are valuable scaffolds, but the direct synthesis of these moieties from terminal alkynes by copper catalysis remains unexplored. We report a robust, general, and efficient method using a simple CuI/2,2'-bipyridine catalytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458563d0be17ad92246b9a7f0f503109
https://doi.org/10.1002/anie.201907448
https://doi.org/10.1002/anie.201907448
Autor:
Katarína Svrčková, Šárka Štěpánková, Jarmila Vinšová, Václav Pflégr, Martin Krátký, Karolína Jaklová
Publikováno v:
Current topics in medicinal chemistry. 20(23)
Background: Development of acetyl- (AChE) and butyrylcholinesterase (BuChE) inhibitors belongs to viable strategies for the treatment of dementia and other diseases related to decrease in cholinergic neurotransmission. Objective: That is why we desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1cc1826e1f5184fb7d879cab865505c
https://pubmed.ncbi.nlm.nih.gov/32814530
https://pubmed.ncbi.nlm.nih.gov/32814530
Autor:
Bastien Michelet, Sébastien Thibaudeau, Sandra Olivero, Ayaka Uehara, Agnès Martin-Mingot, Elisabet Duñach
Publikováno v:
European Journal of Organic Chemistry. 2019:46-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c0ead0399c4fef7e011274b695dc1d
https://doi.org/10.1002/ejoc.201801338
https://doi.org/10.1002/ejoc.201801338