Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marta, Cifuentes García"'
Autor:
José L. García Ruano, Marta Cifuentes García, Angel L. Navarro, Francisco Tato, Ana M. Martín Castro
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 33-45 (2005)
Externí odkaz:
https://doaj.org/article/e34cac1b6ff44e4f9d6a67fcdd6312b5
Autor:
Marta Cifuentes García, José L. García Ruano, Angel L. Navarro, Francisco Tato, Ana M. Martin Castro
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 33-45 (2005)
Results obtained in the reactions of Et2AlCN with exocyclic, endocyclic, and acyclic α-p- tolylsulfinyl ketimines are reported. Good conversions and satisfactory stereochemical results are obtained exclusively from cyclic ketimines. Imine-enamine eq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6c668f58bd8559b540a2f74441d0841
https://doi.org/10.3998/ark.5550190.0006.605
https://doi.org/10.3998/ark.5550190.0006.605
Autor:
Inmaculada Fernández, Jesus H. Rodriguez Ramos, Ana M. Martin Castro, José L. García Ruano, Marta Cifuentes García
Publikováno v:
Tetrahedron: Asymmetry. 9:859-864
Diastereoselective hydrocyanation of enantiomerically pure 2- p -tolylsulfinylacetaldehyde and 2- p -tolylsulfinylpropanal with Et 2 AlCN catalyzed by ZnBr 2 is described. The sulfur configuration controls the stereochemical course of the reaction. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b39d839d53b70acf59932c72af081926
https://doi.org/10.1016/s0957-4166(98)00026-3
https://doi.org/10.1016/s0957-4166(98)00026-3
Autor:
Jose Luis Garcia Ruano, Ana M. Martin Castro, Jesus H. Rodriguez Ramos, Marta Cifuentes García, Nieves M. Laso
Publikováno v:
Angewandte Chemie International Edition. 40:2507-2509
Terminal alkynes are easily transformed into enantiomerically enriched compounds containing tertiary and quaternary carbon atoms. Sulfinylation followed by reduction (or alkylation) and hydrocyanation of the resulting vinyl sulfoxides with Et2 AlCN p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f234ef5e8378e65e54aceefa7a1d789
https://doi.org/10.1002/1521-3773(20010702)40:13<2507::aid-anie2507>3.0.co
https://doi.org/10.1002/1521-3773(20010702)40:13<2507::aid-anie2507>3.0.co
Autor:
Jose Luis Garcia Ruano, Nieves M. Laso, Ana M. Martin Castro, Jesus H. Rodriguez Ramos, Marta Cifuentes García
Publikováno v:
ChemInform. 32
Terminal alkynes are easily transformed into enantiomerically enriched compounds containing tertiary and quaternary carbon atoms. Sulfinylation followed by reduction (or alkylation) and hydrocyanation of the resulting vinyl sulfoxides with Et2 AlCN p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f1b637dab185c41b7c2c34c09acb3df
https://doi.org/10.1002/chin.200141104
https://doi.org/10.1002/chin.200141104
Publikováno v:
ChemInform. 33
Highly enantiopure (R)-2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile 1 (myclobutanil or systhane) was obtained in six synthetic steps from commercially available 1-hexyne (35% yield, 92% ee). The sulfinyl group controls the two key st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385eaabddde38dd0ea761817225b6816
https://doi.org/10.1002/chin.200222132
https://doi.org/10.1002/chin.200222132
Publikováno v:
Organic letters. 4(1)
[reaction: see text] Highly enantiopure (R)-2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile 1 (myclobutanil or systhane) was obtained in six synthetic steps from commercially available 1-hexyne (35% yield, 92% ee). The sulfinyl group co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98893a271743216bc96b70fd75e56f14
https://pubmed.ncbi.nlm.nih.gov/11772089
https://pubmed.ncbi.nlm.nih.gov/11772089
Autor:
Jose L, García Ruano, Marta, Cifuentes García, Nieves M, Laso, Ana M, Martín Castro, Jesús H, Rodríguez Ramos
Publikováno v:
Angewandte Chemie (International ed. in English). 40(13)
Terminal alkynes are easily transformed into enantiomerically enriched compounds containing tertiary and quaternary carbon atoms. Sulfinylation followed by reduction (or alkylation) and hydrocyanation of the resulting vinyl sulfoxides with Et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3187ba651370b186439d5628ba10affe
https://pubmed.ncbi.nlm.nih.gov/29712294
https://pubmed.ncbi.nlm.nih.gov/29712294