Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Maria Elena Meza"'
Publikováno v:
SN Comprehensive Clinical Medicine. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8417e0cd8e727e00f97613d46255953f
https://doi.org/10.1007/s42399-022-01217-x
https://doi.org/10.1007/s42399-022-01217-x
Autor:
Hector Ramon, Martinez Rodriguez1 drhectormtz@yahoo.com, Maria Elena, Meza Cano1
Publikováno v:
Revista Mexicana de Neurociencia. may/jun2016, Vol. 17 Issue 3, p116-123. 8p.
Autor:
Maria Elena, Meza Cano1,2, Talavera Verónica, García2 oksana_12@hotmail.com
Publikováno v:
Revista Mexicana de Neurociencia. may/jun2015, Vol. 16 Issue 3, p52-57. 6p.
Autor:
Arlene A. Sy-Cordero, Nicholas H. Oberlies, Maria Elena Meza Avina, Cedric J. Pearce, Mitchell P. Croatt, Audrey F. Adcock, Mario Figueroa, Huzefa A. Raja, Mansukh C. Wani, David J. Kroll
Publikováno v:
Tetrahedron. 71:8899-8904
Spiroscytalin (1), a new tetramic acid that possesses an uncommon spiro-ring fusion between a polyketide-derived octalin ring system and a 2,4-pyrrolidinedione, along with two known compounds, leporin B (2) and purpactin A (3), were isolated from a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0870e2a812e523936d91f614d57e16f0
https://doi.org/10.1016/j.tet.2015.09.073
https://doi.org/10.1016/j.tet.2015.09.073
Publikováno v:
Tetrahedron. 69:7840-7846
The reactivity of a series of 1,5-disubstituted sulfonyl-triazoles was explored using either thermolytic or metal-catalyzed conditions. Both the thermolysis and the Rh(II)-catalyzed reactions led to the synthesis of a-sulfonyl-nitriles, which presuma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff922c69abe6b327c7a02d7ec1e9269a
https://doi.org/10.1016/j.tet.2013.05.048
https://doi.org/10.1016/j.tet.2013.05.048
Publikováno v:
The Journal of Organic Chemistry. 78:7594-7600
The mechanism for the biomimetic synthesis of flavonolignan diastereoisomers in milk thistle is proposed to proceed by single-electron oxidation of coniferyl alcohol, subsequent reaction with one of the oxygen atoms of taxifolin's catechol moiety, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62631ac98d76286373b750f4453cbbeb
https://doi.org/10.1021/jo4011377
https://doi.org/10.1021/jo4011377
Autor:
Arlene A. Sy-Cordero, Cedric J. Pearce, Mario Figueroa, Maria Elena Meza Avina, Huzefa A. Raja, Mansukh C. Wani, David J. Kroll, Nicholas H. Oberlies, Audrey F. Adcock, Mitchell P. Croatt
Publikováno v:
ChemInform. 47
Compound (I) is shown to exhibit moderate antitumoric activity and no antimicrobial activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d38746ab7845aea27d54994b09bdb04
https://doi.org/10.1002/chin.201610217
https://doi.org/10.1002/chin.201610217
Publikováno v:
Synlett. 23:2869-2874
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nucleophilic alkynes and electrophilic azides to synthesize sulfonyl-substituted 1,5-disubstituted 1,2,3-triazoles. The second method reacts electrophilic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38ce24aa59c7ca61a9cb56faeaf46e25
https://doi.org/10.1055/s-0032-1317545
https://doi.org/10.1055/s-0032-1317545
Autor:
Maria Elena Meza-Aviña, Mitchell P. Croatt, Mudita Kishor Patel, Cylivia B. Lee, Thomas J. Dietz
Publikováno v:
Organic Letters. 13:2984-2987
The reaction of acetylides with sulfonyl azides was found to selectively form 1,5-substituted sulfonyl triazoles. This reaction thus provides access to the regioisomeric product as compared to the popular copper-catalyzed azide-alkyne cycloaddition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd364b7a2c3e4ac014cac1f47e156eae
https://doi.org/10.1021/ol200696q
https://doi.org/10.1021/ol200696q
Autor:
Emil F. Pai, Ian Crandall, Angelica M. Bello, Maria Elena Meza-Aviña, Ewa Poduch, Kevin C. Kain, Lakshmi P. Kotra, Yan Liu, Melissa Maureen Lewis, Lianhu Wei, Christopher J. Paige
Publikováno v:
Journal of Medicinal Chemistry. 54:2891-2901
Fluorinated nucleosides and nucleotides are of considerable interest to medicinal chemists because of their antiviral, anticancer, and other biological activities. However, their direct interactions at target binding sites are not well understood. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f66df55236b962982a7528b236f57077
https://doi.org/10.1021/jm101642g
https://doi.org/10.1021/jm101642g