Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Imanol Tellitu"'
Publikováno v:
ARKIVOC, Vol 2011, Iss 2, Pp 115-126 (2010)
Externí odkaz:
https://doaj.org/article/ec1d457a7dcf4e81b158ae9d723b0176
Publikováno v:
ARKIVOC, Vol 2010, Iss 3, Pp 7-14 (2009)
Externí odkaz:
https://doaj.org/article/4a80f66491fa4f07a97e76782bd81d87
Publikováno v:
ARKIVOC, Vol 2007, Iss 4, Pp 270-278 (2006)
Externí odkaz:
https://doaj.org/article/cadfec9b9c8442609d948ac4f1c3b1b7
Autor:
M. Teresa Herrero, Imanol Tellitu, Susana Hernández, Esther Domínguez, Isabel Moreno, Raúl SanMartín
Publikováno v:
ARKIVOC, Vol 2002, Iss 5, Pp 31-37 (2002)
Externí odkaz:
https://doaj.org/article/a488f07622f84a2fb4a1a0b1c06411c1
Publikováno v:
Tetrahedron. 71:8251-8255
A comparative study of the thermal and microwave-assisted decarboxylation of a series of mono- and disubstituted monohydrolyzed malonate derivatives has been carried out. It has been found out that in both circumstances the use of imidazole has a pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f5fafddce93ab82efdc6960ec422a3e
https://doi.org/10.1016/j.tet.2015.09.012
https://doi.org/10.1016/j.tet.2015.09.012
Publikováno v:
ChemInform. 47
A comparative study of the thermal and microwave-assisted decarboxylation of a series of mono- and disubstituted monohydrolyzed malonate derivatives has been carried out. It has been found out that in both circumstances the use of imidazole has a pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65941c9852b0e247cd8865d19dbb215a
https://doi.org/10.1002/chin.201607070
https://doi.org/10.1002/chin.201607070
Autor:
Imanol Tellitu, Esther Domínguez
Publikováno v:
Synlett. 23:2165-2175
Direct oxidation of suitably functionalized amides by application of the hypervalent iodine reagent PIFA [bis(trifluoroacetoxy)iodo]benzene allows straightforward access to a variety of nitrogen-containing heterocycles. Comprehensive results from o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27a2896509a87ca99c60337d29462fb3
https://doi.org/10.1055/s-0032-1316739
https://doi.org/10.1055/s-0032-1316739
Publikováno v:
Tetrahedron. 68:3692-3700
The construction of the title compounds has been achieved from properly substituted linear alkynylamides through the suitable combination of two key cyclization steps. First, an intramolecular PIFA-mediated alkyne amidation protocol leads to the crea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a077f06a575f99e882fc12f395c2472
https://doi.org/10.1016/j.tet.2012.03.033
https://doi.org/10.1016/j.tet.2012.03.033
Publikováno v:
Synlett. 23:881-884
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::781dae9e11dba653d2f02356774e0772
https://doi.org/10.1055/s-0031-1290604
https://doi.org/10.1055/s-0031-1290604
Publikováno v:
ARKIVOC, Vol 2011, Iss 2, Pp 115-126 (2010)
In this paper it is established a protocol leading to a series of dihydropyrimidine-5-carboxamides under Biginelli reaction conditions starting directly from 3-ketoamides as the 1,3-dicarbonyl component of the process. The best results have been foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b41dcc3348680fb64c7e04f3af01c695
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0012.209
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0012.209