Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Caroline Da Ros Montes D'Oca"'
Autor:
Leice Milla Ribeiro de Novais, Sher Ali, Caroline Da Ros Montes D’Oca, Kahlil Schwanka Salome, Andersson Barison
Publikováno v:
Frontiers in Natural Products, Vol 3 (2024)
IntroductionSome papers describe the presence of creatine in plants, based on a singlet signal at 3.02–3.05 ppm in the 1H NMR spectra. Although is there creatine in plants? Therefore, to answer this question, a comprehensive NMR investigation has b
Externí odkaz:
https://doaj.org/article/5815182a65684105a4163fc8e088580c
Autor:
Sher Ali, Gul Badshah, Caroline Da Ros Montes D’Oca, Francinete Ramos Campos, Noemi Nagata, Ajmir Khan, Maria de Fátima Costa Santos, Andersson Barison
Publikováno v:
Molecules, Vol 25, Iss 16, p 3647 (2020)
Berberis laurina (Berberidaceae) is a well-known medicinal plant used in traditional medicine since ancient times; however, it is scarcely studied to a large-scale fingerprint. This work presents a broad-range fingerprints determination through high-
Externí odkaz:
https://doaj.org/article/46d49f9b93d44229be1d30560315776c
Autor:
Carolina R. Lopes, Caroline Da Ros Montes D'Oca, Rodrigo da C. Duarte, Márcia H. S. Kurz, Ednei G. Primel, Rosilene M. Clementin, Joaquín Ariel M. Villarreyes, Marcelo G. Montes D'Oca
Publikováno v:
Química Nova, Vol 33, Iss 6, Pp 1335-1341 (2010)
Recent biochemical and pharmacological studies have led to the characterization of different fatty acid amides as a new family of biologically active lipids. Here, we describe the synthesis of new amides from C16:0, 18:0, 18:1 and 18:1, OH fatty acid
Externí odkaz:
https://doaj.org/article/f13c2b97e79942f6bc1b679c529c4fa4
Autor:
Elise Ane Maluf Rios, Carla M. B. Gomes, Gabriel L. Silvério, Eduardo Q. Luz, Sher Ali, Caroline da Ros Montes D'Oca, Breidi Albach, Renan B. Campos, Daniel S. Rampon
Publikováno v:
RSC Advances. 13:914-925
We developed a combined experimental and theoretical study that gives mechanistic insights into the silver-catalyzed direct selanylation of indoles.
Autor:
Diego Seckler, Camila M. Dea, Elise Ane Maluf Rios, Marcelo de Godoi, Daniel da Silveira Rampon, Marcelo Gonçalves Montes D’Oca, Caroline Da Ros Montes D'Oca
Publikováno v:
New Journal of Chemistry. 46:4570-4578
WERSA/glycerol is described as a powerful combination for the green approach of the Knoevenagel reaction, without any additional catalyst, base or promoter.
Autor:
Jéssica Thais de Lima, Sônia Faria Zawadzki, Frederico Luis Felipe Soares, Kahlil Schwanka Salome, Andersson Barison, Tiago Bueno de Moraes, Caroline Da Ros Montes D'Oca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a051f65b6a6754beee6c79788446a05b
https://doi.org/10.2139/ssrn.4378149
https://doi.org/10.2139/ssrn.4378149
Autor:
Lucas de Sousa Nascimento, Rogério J. Melo Nascimento, Allann Karlos Alves da Mata, Vinícius Taveira Andrade Felipe, Rayanne Ferreira Araújo, Luiz Carlos Alves Bezerra, Jéssica Silva Almeida, Adriano Lincoln Albuquerque Mattos, Daniel Esdras Andrade Uchoa, Leice Milla Ribeiro de Novais, Caroline Da Ros Montes D'Oca, Francisco Avelino
Publikováno v:
International Journal of Biological Macromolecules. 239:124300
Autor:
Daniel S. Rampon, Eduardo Q. Luz, Caroline da Ros Montes D'Oca, Ronilson Vasconcelos Barbosa, David B. Lima, Diego Seckler, Gabriel L. Silvério, Francielli S. Santana
Publikováno v:
Advanced Synthesis & Catalysis. 363:2610-2618
Autor:
Marcelo Gonçalves Montes D'Oca, Dennis Russowsky, Felipe Ramiro Sobral, Marieli Oliveira Rodrigues, Caroline da Ros Montes D'Oca
Publikováno v:
ChemistrySelect. 5:11921-11926
Autor:
Renata Fontes Ongaratto, Marcelo Gonçalves Montes D'Oca, Caroline Da Ros Montes D’Oca, Arthur Motta de Andrade, Eduardo Bustos Mass, Dennis Russowsky
Publikováno v:
New Journal of Chemistry. 44:13230-13239
In this work, were synthesized for the first time a series of new lipophilic β-alkyl substituted GABA derivatives from fatty alkyl chains. The synthesis of these GABA analogues was investigated by two different bicomponent approaches as a key step.