Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marcos V. M. Teixeira"'
Autor:
Nilo Zanatta, Marcos V. M. Teixeira, Marcos A. P. Martins, Wilson Cunico, Rodrigo L. Peres, Helio G. Bonacorso, Sergio Brondani, Daniel J. Emmerich, Adilson P. Sinhorin, Claudio M. P. Pereira, Paulo Beck
Publikováno v:
Synthetic Communications. 34:1915-1923
A convenient one‐pot synthesis of eight pyrazole‐5(3)‐carboxyamides from the reaction of the 5(3)‐trichloromethylpyrazoles with amines, in good yield, is reported. These reactions show that the trichloromethyl group is a convenient precursor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32ca5d74a0e373be04f73e85745fa804
https://doi.org/10.1081/scc-120034176
https://doi.org/10.1081/scc-120034176
Autor:
Nilo Zanatta, Marcos V. M. Teixeira, Elisandra Scapin, Yao-Feng Yuan, Claudio M. P. Pereira, Helio G. Bonacorso, Wilson Cunico, Clovis Peppe, Rodrigo Mayer, Marcos A. P. Martins
Publikováno v:
Tetrahedron Letters. 45:8991-8994
One-pot condensation of ethyl trichloroacetoacetate 1 with p -substituted aromatic aldehydes (Ph, 4-Me–C 6 H 4 , 4-Cl–C 6 H 4 , 4-MeO–C 6 H 4 ) or furfural, and urea or thiourea catalyzed by indium(III) bromide affords eight trichloromethylated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89005cc4d86864df10f12087a177f4d1
https://doi.org/10.1016/j.tetlet.2004.10.048
https://doi.org/10.1016/j.tetlet.2004.10.048
Autor:
Marcos A. P. Martins, Elisandra Scapin, Rodrigo Mayer, Claudio M. P. Pereira, Yao-Feng Yuan, Wilson Cunico, Nilo Zanatta, Marcos V. M. Teixeira, Clovis Peppe, Helio G. Bonacorso
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb7c323d09806ec7f187121e8c42bc39
https://doi.org/10.1002/chin.200511159
https://doi.org/10.1002/chin.200511159
Autor:
Helio G. Bonacorso, Claudio M. P. Pereira, Paulo Beck, Pablo Machado, Marcos A. P. Martins, Sidnei Moura, Nilo Zanatta, Marcos V. M. Teixeira
Publikováno v:
ChemInform. 34
A series of five 5-trichloromethyl-1-phenyl-1 H -pyrazoles and six 5-trichloromethyl-1,2-dimethylpyrazolium chlorides have been synthesized in 80–98% yield by environmentally benign microwave induced techniques involving the cyclocondensation of 4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5629d5cef2cc87fdd746700fe4962c74
https://doi.org/10.1002/chin.200348117
https://doi.org/10.1002/chin.200348117
Autor:
T. P. Missio, Helio G. Bonacorso, Adilson P. Sinhorin, Patricia D. Sauzem, Nilo Zanatta, Maribel Antonello Rubin, Marcos A. P. Martins, Marcos V. M. Teixeira, Daiane Bolzan Berlese, Zuleica Tabarelli, Carlos Fernando Mello
Publikováno v:
Scopus-Elsevier
Brazilian Journal of Medical and Biological Research, Volume: 37, Issue: 10, Pages: 1531-1540, Published: OCT 2004
Brazilian Journal of Medical and Biological Research, Vol 37, Iss 10, Pp 1531-1540 (2004)
Brazilian Journal of Medical and Biological Research v.37 n.10 2004
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Volume: 37, Issue: 10, Pages: 1531-1540, Published: OCT 2004
Brazilian Journal of Medical and Biological Research, Vol 37, Iss 10, Pp 1531-1540 (2004)
Brazilian Journal of Medical and Biological Research v.37 n.10 2004
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
The antinociceptive effect of six novel synthetic pyrazolines (3-ethoxymethyl-5-ethoxycarbonyl-1H-pyrazole (Pz 1) and its corresponding 1-substituted methyl (Pz 2) and phenyl (Pz 3) analogues, and 3-(1-ethoxyethyl)-5-ethoxycarbonyl-1H-pyrazole (Pz 4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ca157770c91cb15a6e644c52e6f3665
http://www.scopus.com/inward/record.url?eid=2-s2.0-5644245386&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-5644245386&partnerID=MN8TOARS
