Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Monleón Ventura, Alicia"'
Autor:
Monleón Ventura, Alicia
Publikováno v:
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
instname
La adición nucleofílica a los dobles enlaces C=N es uno de los métodos más utilizados para la síntesis de derivados nitrogenados. Sin embargo, supone un desafío sintético debido a la baja electrofilia del átomo de carbono azometínico compara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ad67e74a0a32eac37f4b17facdb7c8db
http://hdl.handle.net/10550/31684
http://hdl.handle.net/10550/31684
Publikováno v:
De Munck, Lode Monleón Ventura, Alicia Vila Descals, Carlos Pedro, José Ramón 2017 Diarylprolinol as a Ligand for Enantioselective Alkynylation of Cyclic Imines Advanced Synthesis & Catalysis 359 9 1582 1587
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
An easily accessible prolinol derived ligand, (S)-bis(3,5-bis(trifluoromethyl)phenyl)(pyrrolidin-2-yl)methanol, has been efficiently applied in the catalytic enantioselective addition of terminal alkynes to cyclic imines using dimethylzinc (Me2Zn) un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f96f8a5d744353fe59a4c224d8da14e4
https://hdl.handle.net/10550/73691
https://hdl.handle.net/10550/73691
Publikováno v:
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
De Munck, Lode Monleón Ventura, Alicia Vila Descals, Carlos Muñoz, M. Carmen Pedro, José Ramón 2015 Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates Organic & Biomolecular Chemistry 13 27 7393 7396
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
De Munck, Lode Monleón Ventura, Alicia Vila Descals, Carlos Muñoz, M. Carmen Pedro, José Ramón 2015 Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates Organic & Biomolecular Chemistry 13 27 7393 7396
RODERIC. Repositorio Institucional de la Universitat de Valéncia
[EN] (R)-VAPOL-Zn(II) complexes catalysed the enantioselective addition of terminal alkynes to cyclic benzoxathiazine 2,2-dioxides, providing the corresponding chiral propargylic sulfamidates with high yields (up to 93%) and good enantiomeric excesse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f42719d9fe6ce857d728cc24fbec9bf