Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mateus L. Stivanin"'
Autor:
Mateus L. Stivanin, Amanda F. da Silva, Alessandra A. G. Fernandes, Igor D. Jurberg, Celso Y. Okada
Publikováno v:
Advanced Synthesis & Catalysis. 362:1106-1111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d741bc81babede814ea9b2d5085cc223
https://doi.org/10.1002/adsc.201901343
https://doi.org/10.1002/adsc.201901343
Publikováno v:
Chemical Society Reviews. 49:6833-6847
Carbenes are important intermediates in organic chemistry and have been widely applied in various types of organic reactions, ranging from cycloaddition reactions and sigmatropic rearrangements to C-H functionalizations, thus allowing the rapid const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27955d8f1104d817dd2b5ab43ec2ed67
https://doi.org/10.1039/d0cs00224k
https://doi.org/10.1039/d0cs00224k
Publikováno v:
The Journal of organic chemistry. 86(23)
Two visible-light-mediated O-H insertion protocols involving oximes and aryldiazoacetates leading to different products depending on the solvent employed are reported. In DCM, direct O-H insertion takes place. In THF, there is the additional incorpor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::122e3bf5b16c26fd682100c9032160cc
https://pubmed.ncbi.nlm.nih.gov/34793163
https://pubmed.ncbi.nlm.nih.gov/34793163
Publikováno v:
ChemistrySelect. 4:3360-3365
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95096593ed5cc89e63d2bee098560ce7
https://doi.org/10.1002/slct.201900761
https://doi.org/10.1002/slct.201900761
Autor:
Samuel Thurow, Alessandra A. G. Fernandes, Igor D. Jurberg, Amanda F. da Silva, Mateus L. Stivanin
Publikováno v:
Synthesis. 50:2473-2489
Isoxazol-5-one rings have been identified as relevant motifs in drug candidates, agrochemicals, and materials. Furthermore, this heterocycle has been also applied as a versatile building block for the preparation of a variety of densely functionalize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b117a2e40b2b1809e6999ef82f3d3ae
https://doi.org/10.1055/s-0036-1589534
https://doi.org/10.1055/s-0036-1589534
Autor:
Camila Sartori, Naylil M. R. Capreti, Marcelo Duarte, Igor D. Jurberg, Mateus L. Stivanin, Célio F. F. Angolini
Publikováno v:
The Journal of organic chemistry. 82(19)
A novel, scalable strategy for the preparation of 2,3,4,6-tetrasubstituted pyridines is described. This protocol has two steps: an aminocatalyzed addition of ketones to alkylidene isoxazol-5-ones, followed by an iron-mediated decarboxylative cyclizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75af0d838e81d90e2d07f4a63caab5aa
https://pubmed.ncbi.nlm.nih.gov/28905627
https://pubmed.ncbi.nlm.nih.gov/28905627