Zobrazeno 1 - 10
of 10
pro vyhledávání: '"João Marcos Batista Junior"'
Autor:
Cintia Duarte de Freitas Milagre, Bruno Sergio do Amaral, João Marcos Batista Junior, Adriana Ferreira Lopes Vilela, Carmen Lúcia Cardoso, Humberto Marcio Santos Milagre
Publikováno v:
Eclética Química, Vol 47, Iss 2, Pp 17-35 (2022)
A chemoenzymatic approach for the synthesis of Alpha-N-heterocyclic ethyl- and phenylacetamides, levetiracetam analogs, is described. Eight nitrile substrates were prepared through the N-alkylation of heterocycles (2-pyrrolidinone, 2-piperidinone, 2-
Externí odkaz:
https://doaj.org/article/9e099bfe16f4408cb32a022310f9b528
Autor:
Andrea Nastri de Luca Batista, João Marcos Batista Junior, Silvia Noelí López, Maysa Furlan, Alberto José Cavalheiro, Dulce Helena Siqueira Silva, Vanderlan da Silva Bolzani, Sergio Massayoshi Nunomura, Massayoshi Yoshida
Publikováno v:
Química Nova, Vol 33, Iss 2, Pp 321-323 (2010)
Phytochemical investigations on three Brazilian Lauraceae species from the Cerrado region of São Paulo State, Ocotea corymbosa (Meins) Mez., O. elegans Mez. and Persea pyrifolia Nees & Mart. ex Nees resulted in the isolation of flavonoids, an ester
Externí odkaz:
https://doaj.org/article/6f462c6d028340babf634b848f5f7a05
Autor:
Tomaz Henrique Duarte Chorro, Edson Leonardo Scarpa de Souza, Otto Daolio Köster, Ellen Christine Polo, Rafaela Costa Carmona, Vitor Hugo Menezes da Silva, João Marcos Batista Junior, Carlos Roque Duarte Correia
Publikováno v:
Advanced Synthesis & Catalysis. 365:211-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a60c27200c963d91ab47d17863c8cf8
https://doi.org/10.1002/adsc.202201313
https://doi.org/10.1002/adsc.202201313
Autor:
Carlos Roque Duarte Correia, Tomaz Chorro, Edson Leonardo Scarpa de Souza, Otto Koster, Ellen Polo, Vitor Hugo da Silva, João Marcos Batista Junior
A new enantioselective intramolecular strategy for the synthesis of enantioenriched bridged benzoxacines, unsaturated spirobenzofurans, methyl-2,3-dihydrobenzofuran acetates, and methyl-2,3-indoline acetate scaffolds in a tandem-like diazotization/He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5f6504b4cf75955b757d742d0b6ce30
https://doi.org/10.26434/chemrxiv-2022-whlz5
https://doi.org/10.26434/chemrxiv-2022-whlz5
Autor:
Quezia Bezerra Cass, Maria Elizabeth Tiritan, João Marcos Batista Junior, Juliana Cristina Barreiro
An expert resource for chemists using stereochemical analysis methods In Chiral Separations and Stereochemical Elucidation: Fundamentals, Methods, and Applications, a team of distinguished researchers delivers a robust and authoritative discussion of
Publikováno v:
Natural Product Reports. 32:1280-1302
Covering: 2000 to 2014 This review covers conformational and configurational assignments in natural product molecules using chiroptical spectroscopy reported over the last 15 years. Special attention is given to vibrational optical activity methods a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd8f8ae231857540f51729bfc3c79c59
https://doi.org/10.1039/c5np00027k
https://doi.org/10.1039/c5np00027k
Autor:
Vanderlan Bolzani, Meri Emili Ferreira Pinto, André Farias de Moura, João Marcos Batista Junior, Kalil Bernardino, Vanderlan Da Silva Bolzani
Publikováno v:
Chemical communications (Cambridge, England). 53(53)
A simple MD-based protocol is presented to accurately predict both the sequence and order of disulfide bond formation in proteins containing multiple cysteine residues. It provides a detailed description of their dynamical and structural features, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b52c8fb008eee9c7e65b46b35d1163d9
https://pubmed.ncbi.nlm.nih.gov/28508909
https://pubmed.ncbi.nlm.nih.gov/28508909
Autor:
Silvia N. Lopez, Vanderlan da Silva Bolzani, Daniela Luz Ambrósio, João Marcos Batista Junior, Luis Octávio Regasini, Maysa Furlan, Adriana A. Lopes, Massuo J. Kato, Regina Maria Barretto Cicarelli
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
This study describes the antichagasic potential of five compounds isolated from leaves of Piper crassinervium (Piperaceae). Two prenylated benzoic acid derivatives, one prenylated hydroquinone and two flavanones, were evaluated. The in vitro trypanoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5daff66cefcb86c75757da147893204
https://doi.org/10.1080/14786410802243271
https://doi.org/10.1080/14786410802243271
Autor:
Vanderlan da Silva Bolzani, João Marcos Batista Junior, Alberto José Cavalheiro, Sergio Massayoshi Nunomura, Maysa Furlan, Massayoshi Yoshida, Dulce Helena Siqueira Silva, Silvia N. Lopez, Andrea N. L. Batista
Publikováno v:
Química Nova, Vol 33, Iss 2, Pp 321-323 (2010)
Repositório Institucional do INPA
Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron:INPA
Química Nova v.33 n.2 2010
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Química Nova, Volume: 33, Issue: 2, Pages: 321-323, Published: 2010
Repositório Institucional do INPA
Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron:INPA
Química Nova v.33 n.2 2010
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Química Nova, Volume: 33, Issue: 2, Pages: 321-323, Published: 2010
Submitted by Guilherme Lemeszenski (guilherme@nead.unesp.br) on 2013-08-22T18:48:49Z No. of bitstreams: 1 S0100-40422010000200017.pdf: 242505 bytes, checksum: 178d6611bc19b0615dbbe4e4a7a24d81 (MD5) Made available in DSpace on 2013-08-22T18:48:49Z (GM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7ba6716427c89aedca83ae662da0623
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000200017
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000200017
Autor:
Jonas da Silva Mota, Regina Maria Barretto Cicarelli, Ana C. Leite, Vanderlan da Silva Bolzani, Maysa Furlan, João Marcos Batista Junior, Daniela Luz Ambrósio, Gabriela Duó Passerini, Silvia N. Lopez, Massuo J. Kato
Publikováno v:
Planta medica. 75(6)
The trypanocidal activity of crude extracts and fractions from the leaves and stems of Peperomia obtusifolia (Piperaceae) was evaluated in vitro against the epimastigote forms of Trypanosoma cruzi. Bioactivity-guided fractionation of the most active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::376ea5e95274e4ee8a4676fc81bfb629
https://pubmed.ncbi.nlm.nih.gov/19241331
https://pubmed.ncbi.nlm.nih.gov/19241331