Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Francisco J. Reboredo"'
Publikováno v:
Synlett. :1603-1606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1c0061e4ac739f820c6fff7f1519301
https://doi.org/10.1055/s-2003-40984
https://doi.org/10.1055/s-2003-40984
Autor:
Ricardo A. Tapia, Francisco J. Reboredo, Cristian O. Salas, Juan C. Estevez, Ramón J. Estévez
Publikováno v:
ChemInform. 41
The preliminary results of a regiospecific synthesis of ( Z)-1-(2-nitrobenzylidene)isochroman-3-onesby gold(I)-catalyzed cycloisomerization of phenylethynylacetic acidsunder mild conditions is described. These novel lactones provedto be suitable star
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48206ab8b6e570a95ad147fd555b2a93
https://doi.org/10.1002/chin.201016101
https://doi.org/10.1002/chin.201016101
Autor:
Juan C. Estevez, Francisco J. Reboredo, Ricardo A. Tapia, Ramón J. Estévez, Cristian O. Salas
Publikováno v:
SYNLETT
Artículos CONICYT
CONICYT Chile
instacron:CONICYT
Artículos CONICYT
CONICYT Chile
instacron:CONICYT
The preliminary results of a regiospecific synthesis of ( Z)-1-(2-nitrobenzylidene)isochroman-3-onesby gold(I)-catalyzed cycloisomerization of phenylethynylacetic acidsunder mild conditions is described. These novel lactones provedto be suitable star
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8251a638f7bdf85f773d542a5136d295
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
instname
The 12th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis We describe herein two synthetic approaches to 3-phenyl-5-nitro-isocoumarines, both based on a nitro-facilitated cyclization of o-phenylethy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483d0095cce9e74783dc0dbcc77b87a4
http://hdl.handle.net/10347/26853
http://hdl.handle.net/10347/26853
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a70dd094864ae07e3c1bbdd07078e19
https://doi.org/10.1002/chin.200402136
https://doi.org/10.1002/chin.200402136
Publikováno v:
ChemInform. 33:129-129
2-(2'-Nitrophenylethynyl)benzoic acid esters, obtained by Sonagashira coupling of o-bromobenzoates to 2-(2'-nitrophenyl)acetylenes, were converted into indeno[1,2-b]indoles by a two-step sequence, through the corresponding 2-nitrophenyl-1,3-indandion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5803224db354c4570b535e6738183e9f
https://doi.org/10.1002/chin.200240129
https://doi.org/10.1002/chin.200240129