Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Mauricio Navarro Villalobos"'
Autor:
Norberto Farfán, María Magdalena Vázquez-Alvarado, Mauricio Navarro Villalobos, Rosa Santillan, Blas Flores-Pérez, Oscar González-Antonio, Margarita Romero-Ávila
Publikováno v:
New Journal of Chemistry. 43:10491-10500
Delving into the scarcely explored versatility and selectivity of 4,7-dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine towards aromatic nucleophilic substitution, eleven new compounds were synthesized using different nucleophiles (alcohols, amines, and thio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c10b01a86915bfcef8c0ca30a2696907
https://doi.org/10.1039/c9nj01855g
https://doi.org/10.1039/c9nj01855g
Publikováno v:
Tetrahedron. 74:5085-5088
Described is a total synthesis of the related alkaloids, cyclopiamide A and speradine E, via a unified strategy that also delivers the natural product aspergilline A. Key steps include metal-free conversion of a malonyl chloride and propargylamine to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bc4d4e5b281d10eaecc527a5d6454b5
https://doi.org/10.1016/j.tet.2018.02.039
https://doi.org/10.1016/j.tet.2018.02.039
Publikováno v:
Organic Letters. 13:1110-1113
In this report, it is demonstrated that chiral vinyl aziridines can be stereospecifically ring expanded. This synthetic approach allows controlled access to chiral 2,5-cis- or 2,5-trans-3-pyrroline products from starting materials with the appropriat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc8845b6a5cc228893dc59dc75d7fd6b
https://doi.org/10.1021/ol200263g
https://doi.org/10.1021/ol200263g
Publikováno v:
Tetrahedron Letters. 50:6450-6453
Model studies towards the total synthesis of syringolides using a rhodium-catalyzed intramolecular C–H insertion reaction as the key step are described. A highly stereospecific synthesis of spirolactones is achieved employing this methodology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fe9a02db80042466e56836531a36e3a
https://doi.org/10.1016/j.tetlet.2009.08.126
https://doi.org/10.1016/j.tetlet.2009.08.126
Autor:
Catherine McCarty, Cristy Lindberg Benson, Mauricio Navarro Villalobos, Steven M. Zeman, Susan Jeong, John L. Wood, Matthew M. Weiss, Analee Salcedo, Jonathan Jenkins
Publikováno v:
Tetrahedron. 65:8091-8098
The first total syntheses of (−)-syringolide 3, (+)-syributin 3 and their unnatural enantiomers (+)-syringolide 3 and (−)-syributin 3 using a common intermediate as starting material are described. In addition, total syntheses of (−)- and (+)-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48c1a1599cd4e255f4dcd3c87dcf2c41
https://doi.org/10.1016/j.tet.2009.07.055
https://doi.org/10.1016/j.tet.2009.07.055
Publikováno v:
ChemInform. 42
In this report, it is demonstrated that chiral vinyl aziridines can be stereospecifically ring expanded. This synthetic approach allows controlled access to chiral 2,5-cis- or 2,5-trans-3-pyrroline products from starting materials with the appropriat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bb5e877a157304e0bd2b6b68e370ec1
https://doi.org/10.1002/chin.201123092
https://doi.org/10.1002/chin.201123092
Publikováno v:
Angewandte Chemie. 113:1162-1164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a090d8f58d30349bbd24c302d6e2fc5
https://doi.org/10.1002/1521-3757(20010316)113:6<1162::aid-ange11620>3.0.co
https://doi.org/10.1002/1521-3757(20010316)113:6<1162::aid-ange11620>3.0.co
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0732d765332a596bfda6f981ea3c49b0
https://doi.org/10.1002/chin.200127214
https://doi.org/10.1002/chin.200127214
Publikováno v:
ChemInform. 41
Model studies towards the total synthesis of syringolides using a rhodium-catalyzed intramolecular C–H insertion reaction as the key step are described. A highly stereospecific synthesis of spirolactones is achieved employing this methodology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0e493126075f173915fc6d8939d3b05
https://doi.org/10.1002/chin.201010106
https://doi.org/10.1002/chin.201010106
Autor:
David Y. Gin, Yong-Jae Kim, JohnMark Derryberry, Bridget D Rohde, Pengfei Wang, Mauricio Navarro-Villalobos
Publikováno v:
Journal of the American Chemical Society. 128(36)
QS-21 is one of the most promising new adjuvants for immune response potentiation and dose-sparing in vaccine therapy given its exceedingly high level of potency and its favorable toxicity profile. Melanoma, breast cancer, small cell lung cancer, pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515dd45792d58c13faa138479d114145
https://pubmed.ncbi.nlm.nih.gov/16953631
https://pubmed.ncbi.nlm.nih.gov/16953631