Zobrazeno 1 - 10
of 14
pro vyhledávání: '"HENRIETE S. VIEIRA"'
Autor:
MARIA AMÉLIA D. BOAVENTURA, LAURA F.W. XAVIER, HENRIETE S. VIEIRA, JACQUELINE A. TAKAHASHI, WILTON J.D. NASCIMENTO JUNIOR, TAMIRES P. ARAUJO, AMANDA C.S. COELHO
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 90, Iss 2 suppl 1, Pp 1945-1954 (2018)
ABSTRACT Thirteen natural products derivatives of hydroxyl amide class, three described for the first time, were synthesized by reaction of three indole acids and 3,4,5-trimethoxybenzoic acid with six different amino alcohols in the presence of triph
Externí odkaz:
https://doaj.org/article/a75bafb342ba426bb9a8795feb9de837
Autor:
Jacqueline A. Takahashi, Henriete S. Vieira, Maria Amélia D. Boaventura, James R. Hanson, Peter B. Hitchcock, Alaíde B. de Oliveira
Publikováno v:
Química Nova, Vol 24, Iss 5, Pp 616-618 (2001)
Externí odkaz:
https://doaj.org/article/baf75092516c4dc69808183c66a0131d
Autor:
Rosana Zacarias Domingues, Jorge L. López, Tulio Matencio, Humberto O. Stumpf, Junnia Alvarenga de Carvalho Oliveira, Jacqueline A. Takahashi, Ângela Leão Andrade, Luciano R. S. Lara, Rosangela Maria Ferreira da Costa e Silva, Henriete S. Vieira
Publikováno v:
Journal of the Brazilian Chemical Society, Volume: 29, Issue: 12, Pages: 2636-2645, Published: DEC 2018
Repositório Institucional da UFOP
Universidade Federal de Ouro Preto (UFOP)
instacron:UFOP
Journal of the Brazilian Chemical Society v.29 n.12 2018
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Repositório Institucional da UFOP
Universidade Federal de Ouro Preto (UFOP)
instacron:UFOP
Journal of the Brazilian Chemical Society v.29 n.12 2018
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
A novel, fast, low-cost and scalable methodology to prepare stable magnetoliposomes (MGLs), without the use of organic solvents, is described. The concept of the work is based on the dual use of soy lecithin associated to a new liposome preparation m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cc2359ec91627eb136fe2e2057e210a
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018001202636&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018001202636&lng=en&tlng=en
Autor:
Laura F W Xavier, Jacqueline A. Takahashi, Maria Amélia D. Boaventura, Amanda Cristina Soares Coelho, Tamires P Araujo, Henriete S. Vieira, Wilton J D Nascimento Junior
Publikováno v:
Anais da Academia Brasileira de Ciências, Issue: ahead, Published: 25 JUN 2018
Anais da Academia Brasileira de Ciências, Vol 90, Iss 2 suppl 1, Pp 1945-1954 (2018)
Anais da Academia Brasileira de Ciências v.90 n.2 suppl.1 2018
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Anais da Academia Brasileira de Ciências, Volume: 90, Issue: 2 Supplement 1, Pages: 1945-1954, Published: 25 JUN 2018
Anais da Academia Brasileira de Ciências, Vol 90, Iss 2 suppl 1, Pp 1945-1954 (2018)
Anais da Academia Brasileira de Ciências v.90 n.2 suppl.1 2018
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Anais da Academia Brasileira de Ciências, Volume: 90, Issue: 2 Supplement 1, Pages: 1945-1954, Published: 25 JUN 2018
Thirteen natural products derivatives of hydroxyl amide class, three described for the first time, were synthesized by reaction of three indole acids and 3,4,5-trimethoxybenzoic acid with six different amino alcohols in the presence of triphenylphosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::033ee949b408ca9bec6962638250e57b
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652018005011106&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652018005011106&lng=en&tlng=en
Autor:
Henriete S. Vieira, Lichang Yin, Clascídia A. Furtado, Marcos A. Pimenta, Cristiano Fantini, Marcela M. Oliveira, Riichiro Saito, Adelina P. Santos, Daniel M. Andrada
Publikováno v:
Carbon. 56:235-242
Raman spectra of octadecylamine (ODA) molecules covalently bound to the surface of single walled carbon nanotubes were obtained by varying the laser excitation energy from 1.92 to 3.81 eV. A strong dependence of the Raman intensity on the excitation
Autor:
Henriete S. Vieira, Luiza Baptista de Oliveira Freitas, Maria Amélia D. Boaventura, Rondinelle Gomes Pereira, Leandro Alves dos Reis
Publikováno v:
Journal of Agricultural and Food Chemistry. 56:2985-2988
Novel kaurane ditepene monoamides were synthesized in good yields directly from kaurenoic ( 1) and grandiflorenic ( 2) acids and unprotected symmetrical diamines, using a modified protocol for monoacylation. Amides from 1 and 2 and monoamines were al
Autor:
A. A. Leslie Gunatilaka, Henriete S. Vieira, Jacqueline A. Takahashi, Maria Amélia D. Boaventura
Publikováno v:
Magnetic Resonance in Chemistry. 44:146-150
A highly rearranged novel dilactone was the single product isolated from Baeyer-Villiger oxidation of a norketone prepared from grandiflorenic acid, a natural kaurane diterpene. The complete 1H and 13C NMR assignment is presented for this novel compo
Autor:
Maria Amélia D. Boaventura, Jacqueline A. Takahashi, Henriete S. Vieira, Lúcia Pinheiro Santos Pimenta
Publikováno v:
Zeitschrift für Naturforschung C. 60:72-78
Kaurenoic and grandiflorenic acid, isolated from Wedelia paludosa (Asteraceae), some derivatives from these acids (alcohols, esters, amides, lactones, oximes) and other naturally occurring kaurane diterpenes were tested for their action on the growth
Publikováno v:
Journal of Agricultural and Food Chemistry. 50:3704-3707
In the search for new routes in the synthesis of hydroxylated kaurane diterpenoids, Verticillium lecanii, grown in a mineral liquid medium for 48 h, was fed with ent-17,19-dihydroxy-16betaH-kaurane, obtained by hydroboration/oxidation of kaurenoic ac
Autor:
Egler Chiari, Maria Amélia D. Boaventura, Alaíde Braga de Oliveira, Henriete S. Vieira, Jacqueline A. Takahashi
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 13, Iss 2, Pp 151-157 (2002)
Journal of the Brazilian Chemical Society, Volume: 13, Issue: 2, Pages: 151-157, Published: 2002
Journal of the Brazilian Chemical Society v.13 n.2 2002
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Volume: 13, Issue: 2, Pages: 151-157, Published: 2002
Journal of the Brazilian Chemical Society v.13 n.2 2002
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Kaurenoic acid, a kauranic diterpenoid, presents in vitro activity against trypomastigote forms of Trypanosoma cruzi, showing, however, lytic activity on blood erythrocytes, as a side effect. The syntheses of twelve new derivatives of kaurenoic acid,