Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Juan Manuel Romo"'
Publikováno v:
European Journal of Organic Chemistry. 2019:6296-6305
Publikováno v:
Organic Letters. 18:3018-3021
A concise synthesis of the C9-C19 fragment of peloruside A that is both highly stereoselective and efficient is described. Achieving an overall yield of 23% over 14 steps, this synthesis not only is high yielding but also involves four chromatography
Autor:
Juan Manuel Romo, Javier Fernández-Valparís, Pedro Romea, Mercè Font-Bardia, Fèlix Urpí, Hubert Kowalski
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
The structurally simple (Me3P)2NiCl2 complex catalyzes SN1-type alkylations of chiral N-acyl thiazolidinethiones with diarylmethyl methyl ethers and other stable carbenium cations. The former can contain a variety of functional groups and heteroatoms
Autor:
Mercè Font-Bardia, Pedro Romea, Stuart C. D. Kennington, Juan Manuel Romo, Fèlix Urpí, Mònica Mato Ferré
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Direct nickel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commercially available nickel(II) complex, (Me3P)2NiCl2, has been developed for tropylium and trityl tetrafluoroborate salts. The reaction provides a s
Autor:
Mercè Font-Bardia, Juan Manuel Romo, Pedro Romea, Javier Fernández-Valparís, Fèlix Urpí, Hubert Kowalski
Publikováno v:
ChemInform. 46
The structurally simple (Me3P)2NiCl2 complex catalyzes SN1-type alkylations of chiral N-acyl thiazolidinethiones with diarylmethyl methyl ethers and other stable carbenium cations. The former can contain a variety of functional groups and heteroatoms
Autor:
Juan Manuel Romo, Ricard Solà, Pedro Romea, Miquel Pellicena, Mercè Font-Bardia, Fèlix Urpí, Alejandro Gómez-Palomino
Publikováno v:
ChemInform. 46
Conversion of chiral N-acyl-4-benzyl-oxazolidinones (I) to titanium enolates and subsequent quenching with TEMPO results in an efficient formation of 2-aminoxylation adducts in excellent yields and good enantioselectivities.
Autor:
Pedro Romea, Miquel Pellicena, Alejandro Gómez-Palomino, Juan Manuel Romo, Mercè Font-Bardia, Fèlix Urpí, Ricard Solà
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
A highly efficient and straightforward aminoxylation of titanium(IV) enolates from (S)-N-acyl-4-benzyl-5,5-dimethyl-1,3-oxazolidin-2-ones with TEMPO has been developed. A wide array of functional groups on the acyl moiety, including alkyl and aryl su
Autor:
Conforti, María Eugenia, Mariano, Mercedes, Lomana, Juan Carlos Díez Fernandez, Endere, María Luz
Publikováno v:
Patrimônio e Memória; v. 15, n. 1 (2019): PATRIMÔNIO E MEMÓRIA; 367-387
Patrimônio e Memória
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Patrimônio e Memória
Universidade Estadual Paulista (UNESP)
instacron:UNESP
En este trabajo se presentan las opiniones divergentes de los habitantes de dos localidades adyacentes al sitio arqueológico del Patrimonio Mundial “Sierra de Atapuerca”. Los resultados mostraron diferencias entre los habitantes de las dos ciuda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::006266acaa0b783df3ea68455016898c
http://pem.assis.unesp.br/index.php/pem/article/view/942
http://pem.assis.unesp.br/index.php/pem/article/view/942