Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Francisca Martín-Gálvez"'
Autor:
Antonio Sánchez-Ruiz, Francisca Martín-Gálvez, Francisco Sarabia, Frederick A. Valeriote, Cristina García-Ruiz
Publikováno v:
ChemMedChem. 8:819-831
Based on our previously described synthetic strategy for bengamide E, a natural product of marine origin with antitumor activity, a small library of analogues modified at the terminal olefinic position was generated with the objective of investigatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1cdad9c178dda50dac4f55927f2d950
https://doi.org/10.1002/cmdc.201300033
https://doi.org/10.1002/cmdc.201300033
Autor:
Francisca Martín-Gálvez, José F. Tejón-Blanco, Samy Chammaa, Miguel Garcia‐Castro, Francisco Sarabia, Antonio Sánchez-Ruiz
Publikováno v:
The Journal of Organic Chemistry. 73:8979-8986
A new approach to the stereoselective synthesis of polypropionate-type frameworks is reported utilizing reactions of amide-stabilized sulfur ylides with chiral aldehydes. To establish a new strategy for macrolide fragment synthesis, the stereoselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c0d22456cc7f413aff7d20c9e383689
https://doi.org/10.1021/jo801728s
https://doi.org/10.1021/jo801728s
Autor:
Francisca Martín-Gálvez, Carlos Vivar-García, Francisco Sarabia, Antonio Sánchez-Ruiz, Cristina García-Ruiz
Publikováno v:
The Journal of organic chemistry. 78(11)
With the objective of investigating the influence of structural modifications of the polyketide chain of the bengamides upon their antitumoral activities, we targeted the preparation of bengamide E analogues with modification of the stereochemistry a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2f2491833d1d0ff3b1505392f6f1b8d
https://pubmed.ncbi.nlm.nih.gov/23647394
https://pubmed.ncbi.nlm.nih.gov/23647394
Autor:
Francisca Martín-Gálvez, Miguel Garcia‐Castro, Samy Chammaa, Francisco Sarabia, Cristina García-Ruiz, Carlos Vivar-García, Antonio Sánchez-Ruiz
Publikováno v:
ChemInform. 44
Ylides, generated in situ by the basic treatment of chiral bicyclic sulfonium salts (I) and (II) react with a large variety of aliphatic, aromatic, heteroaromatic, α,β-unsaturated and chiral functionalized aldehydes to trans-epoxy amides with good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27aae6a9fe2ce24c0dba12a9a5e2dfae
https://doi.org/10.1002/chin.201316068
https://doi.org/10.1002/chin.201316068
Autor:
Carlos Vivar-García, Cristina García-Ruiz, Samy Chammaa, Miguel Garcia‐Castro, Antonio Sánchez-Ruiz, Francisca Martín-Gálvez, Francisco Sarabia
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 18(47)
A new type of chiral sulfonium salts that are characterized by a bicyclic system has been designed and synthesized from α-amino acids. Their corresponding ylides, which were prepared by basic treatment of the sulfonium salts, reacted smoothly with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f764d2fb2003a08a30fd27d1ac4be7d4
https://pubmed.ncbi.nlm.nih.gov/23081826
https://pubmed.ncbi.nlm.nih.gov/23081826
Autor:
Francisca Martín-Gálvez, Samy Chammaa, Antonio Sánchez-Ruiz, Laura Martín-Ortiz, Francisco Sarabia
Publikováno v:
The Journal of organic chemistry. 75(16)
A new synthetic methodology of asymmetric epoxidation developed in our laboratories has been employed for the stereoselective synthesis of bengamide E (16) and analogues at the terminal olefinic position. In the event, the chiral sulfonium salt 30 wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::665c410fa6583be274b0b2718bc22072
https://pubmed.ncbi.nlm.nih.gov/20704428
https://pubmed.ncbi.nlm.nih.gov/20704428
Publikováno v:
ChemInform. 41
A new type of chiral sulfur ylides has been synthesized and their reactivities against carbonyl compounds tested, showing a high degree of stereoselectivity in the formation of transepoxyamides under very mild reaction conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66a50a5bd58bd7ac529a16f18019f007
https://doi.org/10.1002/chin.201007040
https://doi.org/10.1002/chin.201007040
Autor:
Antonio Romero-Carrasco, Carlos Vivar-García, Francisco Sarabia, Antonio Sánchez-Ruiz, Francisca Martín-Gálvez, Cristina García-Ruiz
Publikováno v:
The Journal of Organic Chemistry. 77:9932-9932
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d10e8c8c758f3da1eac54641c3c0fbed
https://doi.org/10.1021/jo300677f
https://doi.org/10.1021/jo300677f