Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lidia Beiza-Granados"'
Autor:
Martín A. Lerma-Herrera, Lidia Beiza-Granados, Alejandra Ochoa-Zarzosa, Joel E. López-Meza, Pedro Navarro-Santos, Rafael Herrera-Bucio, Judit Aviña-Verduzco, Hugo A. García-Gutiérrez
Publikováno v:
Molecules, Vol 27, Iss 12, p 3937 (2022)
Different ethnomedicinal studies have investigated the relationship between various phytochemicals as well as organic extracts and their bioactive aspects. Studies on biological effects are attributed to secondary metabolites such as alkaloids, pheno
Externí odkaz:
https://doaj.org/article/dd28d4fbbaaf48ab96ff73587f659c61
Autor:
Alejandra Ochoa-Zarzosa, Lidia Beiza‐Granados, Joel E. López-Meza, Juan D. Hernández-Hernández, Martín A. Lerma-Herrera, Hugo A. García-Gutiérrez, Judit A. Aviña-Verduzco
Publikováno v:
Saudi Journal of Biological Sciences
Saudi Journal of Biological Sciences, Vol 28, Iss 12, Pp 7082-7089 (2021)
Saudi Journal of Biological Sciences, Vol 28, Iss 12, Pp 7082-7089 (2021)
The aim of this study was to evaluate the cytotoxic potential of Aristolochia foetida Kunth. Stems and leaves of A. foetida Kunth (Aristolochiaceae) have never been investigated pharmacologically. Recent studies of species of the Aristolochiaceae fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0affe22beee7991ad54fd6f79370f5ee
http://europepmc.org/articles/PMC8626259
http://europepmc.org/articles/PMC8626259
Autor:
Hugo A. García-Gutiérrez, Juan D. Hernández-Hernández, Luisa U. Román-Marín, Carlos M. Cerda-García-Rojas, Ángel A. del Río‐Chávez, Pedro Joseph-Nathan, Lidia Beiza‐Granados
Publikováno v:
Chirality. 31:934-946
The epimeric diterpenes (+)-(1S,3E,7E,11S,12S)-verticilla-3,7-dien-12-ol (1), isolated from Bursera suntui, and (+)-(1S,3E,7E,11S,12R)-verticilla-3,7-dien-12-ol (2), isolated from Bursera kerberi, gave the same Wagner-Meerwein rearrangement product (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca79688b07b63e4f8f480901ddb6bf75
https://doi.org/10.1002/chir.23061
https://doi.org/10.1002/chir.23061
Autor:
Rafael Herrera-Bucio, Freddy G. Morales‐Palacios, Lidia Beiza‐Granados, Hugo A. García-Gutiérrez, Pedro Navarro-Santos, José L. Rivera
Publikováno v:
Journal of Physical Organic Chemistry. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b613de30e81a5a8c69a46bdaf6f19ec
https://doi.org/10.1002/poc.4011
https://doi.org/10.1002/poc.4011
Autor:
Pedro Joseph-Nathan, Lidia Beiza-Granados, Oscar R. Suárez-Castillo, J.Roberto Villagómez-Ibarra, Yaneth M. A. Contreras‐Martinez, J. Martín Torres-Valencia, Myriam Meléndez-Rodríguez, Martha S. Morales-Ríos
Publikováno v:
Tetrahedron. 61:8809-8820
The synthesis of N-carbomethoxy-2-alkoxyindolenines and the transformation to their tautomeric indoles is reported. Variable-temperature 1H NMR studies of these 2-alkoxyindolenines evidenced dynamic processes involving two low-energy E and Z equilibr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d43c95fd32649851e7ce9c103f25f16
https://doi.org/10.1016/j.tet.2005.07.023
https://doi.org/10.1016/j.tet.2005.07.023
Autor:
Oscar R, Suárez-Castillo, Myriam, Meléndez-Rodríguez, Lidia, Beiza-Granados, Indira C, Cano-Escudero, Martha S, Morales-Ríos, Pedro, Joseph-Nathan
Publikováno v:
Natural product communications. 6(4)
An efficient route to natural occurring methyl 6-bromoindolyl-3-acetate 1c from methyl indolyl-3-acetate 3 was achieved in 3 steps and 68% overall yield. Thus, in order to regioselectively brominate 3 at the C6-position, introduction of electron with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96e099acfe03cd4109318531341e05aa
https://pubmed.ncbi.nlm.nih.gov/21560757
https://pubmed.ncbi.nlm.nih.gov/21560757
Autor:
Oscar R. Suárez-Castillo, Lidia Beiza-Granados, Alejandro Alvarez-Hernández, Pedro Joseph-Nathan, Myriam Meléndez-Rodríguez, Martha S. Morales-Ríos
Publikováno v:
Journal of natural products. 69(11)
A regioselective synthesis of N-carbomethoxy-2,3,5-tribromoindole (6) via a sequential one-pot bromination−aromatization−bromination of N-carbomethoxyindoline (2) is described. The process for the transformation of 2 into 6 permitted the isolatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b95a189446f889419139f9ede0d9e51
https://pubmed.ncbi.nlm.nih.gov/17125228
https://pubmed.ncbi.nlm.nih.gov/17125228
Autor:
Myriam Meléndez-Rodríguez, Martha S. Morales-Ríos, Oscar R. Suárez-Castillo, Indira C. Cano-Escudero, Pedro Joseph-Nathan, Lidia Beiza-Granados
Publikováno v:
Natural Product Communications. 6:1934578X1100600
An efficient route to natural occurring methyl 6-bromoindolyl-3-acetate 1c from methyl indolyl-3-acetate 3 was achieved in 3 steps and 68% overall yield. Thus, in order to regioselectively brominate 3 at the C6-position, introduction of electron with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91582e350a51bac97cf011dd50ca235b
https://doi.org/10.1177/1934578x1100600405
https://doi.org/10.1177/1934578x1100600405