Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Luis A. Polindara-García"'
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a2228d2f93ef2c9dd80321d38a302ae
https://doi.org/10.1002/ejoc.202101517
https://doi.org/10.1002/ejoc.202101517
Publikováno v:
The Journal of Organic Chemistry. 84:12809-12834
The development of a novel protocol for the fast introduction of the picolinamide directing group in aliphatic ketones by using the ammonia–Ugi 4-CR reaction and the subsequent evaluation of the Pd-mediated γ-C(sp3)–H bond activation is describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c19cff0835afd98f055d1b551ab2105
https://doi.org/10.1021/acs.joc.9b01436
https://doi.org/10.1021/acs.joc.9b01436
Publikováno v:
European Journal of Organic Chemistry. 2019:2453-2471
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f793dee468d85c0601bbde64d4e66a3f
https://doi.org/10.1002/ejoc.201801871
https://doi.org/10.1002/ejoc.201801871
Autor:
Andrés Borja-Miranda, Fabiola Valencia-Villegas, Luis A. Polindara-García, J. Armando Lujan-Montelongo
Publikováno v:
The Journal of organic chemistry. 86(1)
The development of an efficient method for the synthesis of polysubstituted isoindolinones from 1,3-dicarbonyl Ugi-4CR adducts, employing an aromatic radical cyclization process promoted by tetrabutylammonium persulfate and 2,2,6,6-tetramethyl-1-pipe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862a36d095515432e621260be681b6ba
https://pubmed.ncbi.nlm.nih.gov/33291875
https://pubmed.ncbi.nlm.nih.gov/33291875
Autor:
Carolina Silva-Cuevas, Humberto L. Mendoza-Figueroa, Luis A. Polindara-García, Jesus Armando Lujan-Montelongo, Saray Oliveros-Cruz, Anahí C. Sánchez-Chávez, Mario D. Torres-Cardona
Publikováno v:
Tetrahedron Letters. 59:4096-4101
Lutein, a xanthophyll carotenoid abundant in marigold flowers (Tagetes spp.), is found in the form of ester derivatives of fatty acids. Herein we present an enzymatic approach for the regioselective synthesis of 3-O-acyl monoester lutein derivatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac51f8215283ca10ef215fe330d49c91
https://doi.org/10.1016/j.tetlet.2018.10.006
https://doi.org/10.1016/j.tetlet.2018.10.006
Publikováno v:
European Journal of Organic Chemistry. 2018:4586-4591
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2acd98188bd93bbcaeac63c2a50e12a4
https://doi.org/10.1002/ejoc.201800756
https://doi.org/10.1002/ejoc.201800756
Autor:
Anahí C. Sánchez-Chávez, Mario D. Torres-Cardona, Humberto L. Mendoza-Figueroa, Luis A. Polindara-García, Saray Oliveros-Cruz, J. Armando Lujan-Montelongo
Publikováno v:
European Journal of Organic Chemistry. 2018:3202-3210
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdb6b83a0a5deddd241ee9969987a6c6
https://doi.org/10.1002/ejoc.201800244
https://doi.org/10.1002/ejoc.201800244
Autor:
J. Armando Lujan-Montelongo, Carolina Silva-Cuevas, Luis A. Polindara-García, Carlos Perez-Arrieta
Publikováno v:
Tetrahedron Letters. 58:2244-2247
A rapid and facile method provides a general route to sulfonyl bromides/chlorides by the oxidation of thiols using NXS – ROH (X = Br,Cl, R = i Pr) as an oxyhalogenation reagent. Control experiments suggest that the alcohol component is the source o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::676d11d6497ac95ed70eac7dc7ab3e70
https://doi.org/10.1016/j.tetlet.2017.04.087
https://doi.org/10.1016/j.tetlet.2017.04.087
Publikováno v:
The Journal of organic chemistry. 84(20)
The development of a novel protocol for the fast introduction of the picolinamide directing group in aliphatic ketones by using the ammonia-Ugi 4-CR reaction and the subsequent evaluation of the Pd-mediated γ-C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d3b57db628cb59235b436e52e18cd19
https://pubmed.ncbi.nlm.nih.gov/31385503
https://pubmed.ncbi.nlm.nih.gov/31385503
Publikováno v:
European Journal of Organic Chemistry. 2016:1095-1102
The successful application of a mechanochemical activation strategy that employs high-speed ball milling (HSBM) conditions for isocyanide-based multicomponent reactions (IMCRs) was developed. The syntheses of valuable Ugi (by a liquid-assisted grindi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::556ef88ef59f221530d367fb9c87b032
https://doi.org/10.1002/ejoc.201501371
https://doi.org/10.1002/ejoc.201501371