Zobrazeno 1 - 10
of 19
pro vyhledávání: '"M. Teresa Peromingo"'
Autor:
David Cruz, Francisco Yuste, Jose Luis Garcia Ruano, M. Rosario Martín, Marina Alonso, Alberto Fraile, Amelia Tito, M. Teresa Peromingo
Publikováno v:
Tetrahedron. 64:10546-10551
The reactions of diazomethane, diazoethane, and (trimethylsilyl)diazomethane with (S)-2-p-tolylsulfinylcyclopent-2-en-1-one have been studied. The sulfinyl group increases the reactivity and controls the π-facial and endo/exo selectivities. The π-f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb01b8f2a99310cf108950221728b1f
https://doi.org/10.1016/j.tet.2008.08.088
https://doi.org/10.1016/j.tet.2008.08.088
Publikováno v:
ChemInform. 33
The first 1,3-dipolar reaction of azomethine ylides with optically pure vinyl sulfoxide are reported. The presence of the sulfinyl group increase the reactivity of the acrylate moiety as a dipolarophile, and the reactions evolve with complete regio-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433ba04b7b4164b857430a2062be7d23
https://doi.org/10.1002/chin.200230132
https://doi.org/10.1002/chin.200230132
Autor:
Marina Alonso, M. Teresa Peromingo, Francisco Yuste, Jose Luis Garcia Ruano, David Cruz, Alberto Fraile, M. Rosario Martín, Amelia Tito
Publikováno v:
ChemInform. 40
The reactions of diazomethane, diazoethane, and (trimethylsilyl)diazomethane with (S)-2-p-tolylsulfinylcyclopent-2-en-1-one have been studied. The sulfinyl group increases the reactivity and controls the π-facial and endo/exo selectivities. The π-f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9078c9e919a046b7590adec8c0c73b81
https://doi.org/10.1002/chin.200911037
https://doi.org/10.1002/chin.200911037
Autor:
Angel E. Lozano, María-José Camarasa, Sonsoles Velázquez, Sonia de Castro, M. Teresa Peromingo
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 14(31)
The reactivity of the 4-amino-5H-1,2-oxathiole-2,2-dioxide (or beta-amino-gamma-sultone) heterocyclic system has scarcely been studied. Here we describe the reactivity of this system towards electrophiles and amines on readily available model substra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba1a0710b5256296777a343e4657f481
https://pubmed.ncbi.nlm.nih.gov/18780390
https://pubmed.ncbi.nlm.nih.gov/18780390
Autor:
María-José Camarasa, M. Teresa Peromingo, Graciela Andrei, Robert Snoeck, Sonia de Castro, Lieve Naesens, Jan Balzarini, Sonsoles Velázquez
Publikováno v:
Journal of medicinal chemistry. 51(18)
Analogues of the 4"-benzoyl-ureido-TSAO derivative (1) modified at different positions have been prepared and evaluated against wild-type strains of HCMV and murine cytomegalovirus (MCMV) in cell culture. In addition, the activity of the most active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e875c360901b9a86795d8590f5f60ee
https://pubmed.ncbi.nlm.nih.gov/18707089
https://pubmed.ncbi.nlm.nih.gov/18707089
Publikováno v:
Organic letters. 8(15)
[Structure: see text] Chemoselective and completely stereoselective denitrogenation of optically pure pyrazolines, derived from 3-sulfinylfuran-2(5H)-ones, into cyclopropanes can be achieved under substoichiometric Yb(OTf)3 catalysis. Reactions evolv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6222912360e7af34e5f2770a2e6e434a
https://pubmed.ncbi.nlm.nih.gov/16836389
https://pubmed.ncbi.nlm.nih.gov/16836389
Autor:
Marina Alonso, M. Rosario Martín, Alberto Fraile, Amelia Tito, M. Teresa Peromingo, José L. García Ruano
Publikováno v:
The Journal of organic chemistry. 70(22)
[reaction: see text] The reactions of diazomethane and diazoethane with (S)-3-p-tolylsulfinylfuran-2(5H)-one (3) and its 4-methyl derivative (4) have been studied. The sulfinyl group was able to completely control the pi-facial selectivity of all the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f4367f329738a632c26a1d7867d6e78
https://pubmed.ncbi.nlm.nih.gov/16238331
https://pubmed.ncbi.nlm.nih.gov/16238331
Publikováno v:
The Journal of organic chemistry. 68(26)
Azomethine ylides, derived from iminoesters 1 and DBU in the presence of silver salts, react with (S)-2-p-tolylsulfinyl-2-cyclopentenone 2 in a completely regio- and endoselective manner but with a low facial selectivity, affording a mixture of two c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1b327bc048098261315ae16932a48a
https://pubmed.ncbi.nlm.nih.gov/14682695
https://pubmed.ncbi.nlm.nih.gov/14682695
Publikováno v:
The Journal of organic chemistry. 67(3)
The first 1,3-dipolar reaction of azomethine ylides with optically pure vinyl sulfoxide are reported. The presence of the sulfinyl group increase the reactivity of the acrylate moiety as a dipolarophile, and the reactions evolve with complete regio-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8352765955555e30a2216793b6bab51
https://pubmed.ncbi.nlm.nih.gov/11856048
https://pubmed.ncbi.nlm.nih.gov/11856048
Autor:
Amelia Tito, Alberto Fraile, José L. García Ruano, Rosario Martín, M. Teresa Peromingo, Marina Alonso
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 180:1441-1442
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::796efcefd0d76c33b19f7f23d0e16522
https://doi.org/10.1080/10426500590912998
https://doi.org/10.1080/10426500590912998