Zobrazeno 1 - 10
of 245
pro vyhledávání: '"Bosco, Marcella"'
Autor:
Rabanus, Stefan
Publikováno v:
Zeitschrift für Dialektologie und Linguistik, 2012 Jan 01. 79(2), 195-198.
Externí odkaz:
https://www.jstor.org/stable/24547799
Autor:
Machteld Meulleman
Publikováno v:
HAL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::210b7c041932531227d19fac3a4186e5
https://hal.univ-reims.fr/hal-02473550
https://hal.univ-reims.fr/hal-02473550
Autor:
Bartoli, Giuseppe, Bellucci, M.Cristina, Bosco, Marcella, Dalpozzo, Renato, Marcantoni, Enrico, Sambri, Letizia
Publikováno v:
In Tetrahedron Letters 1999 40(14):2845-2848
Autor:
de Paula Eccard, Camila camilaeccard@gmail.com, Mina Candreva, Hosana hosanaminac@gmail.com, Bosco, Juliana julianabosco.s@gmail.com, Donato Costa, Marcella mdcnit@yahoo.com.br, Carolina Araújo, Ana carol_sg@hotmail.com, Santos Soares, Sarah soares.santos.sarah@gmail.com, Souza, Luciana luli.souza@yahoo.com.br, Ribeiro Soares, Andrea andrearsoares@hotmail.com, Solza, Cristiana csolza@hotmail.com, Rafael Baptista, Renata Lyrio renata.lyrio@outlook.com
Publikováno v:
Brazilian Journal of Health & Biomedical Sciences. 2024 Supplement, Vol. 23, p97-97. 1p.
Autor:
BARTOLI, GIUSEPPE, BOSCO, MARCELLA, CARLONE, ARMANDO, PESCIAIOLI, FABIO, SAMBRI, LETIZIA, MELCHIORRE, PAOLO
The first general and highly enantioselective organocatalytic Friedel-Crafts alkylation of indoles with simple unsaturated ketones has been accomplished. Central to these studies has been the identification of a new catalyst amine salt, in which both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::22821d6432fe6633774f95ed3fb0e4da
http://hdl.handle.net/11585/47316
http://hdl.handle.net/11585/47316
The first organocatalytic asymmetric functionalization of aldehydes with a P-based compound has been successfully developed; the use of a simple chiral secondary amine has enabled the highly chemo- and enantioselective conjugate addition of diphenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::4f89bf08a18b98b92d45b5b79aaf4944
http://hdl.handle.net/11585/47315
http://hdl.handle.net/11585/47315
Autor:
CARLONE, ARMANDO, BARTOLI, GIUSEPPE, BOSCO, MARCELLA, PESCIAIOLI, FABIO, SAMBRI, LETIZIA, MELCHIORRE, PAOLO, P. Ricci
The highly enantioselective organocatalytic β-hydroxylation of α,β-unsaturated ketones has been accomplished using oximes as the oxygen-centered nucleophile. Optically active products are obtained with enantioselectivity up to 94%. Central to thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::9184c5e3092d7490c4ed6a03070823da
http://hdl.handle.net/11585/56216
http://hdl.handle.net/11585/56216
Autor:
BARTOLI, GIUSEPPE, BOSCO, MARCELLA, CARLONE, ARMANDO, LOCATELLI, MANUELA, MELCHIORRE, PAOLO, PALAZZI, PAOLO, SAMBRI, LETIZIA, E. Marcantoni
A new, general and mild method for the direct synthesis of aryl and alkyl ethyl carbonates promoted by a Lewis acid is reported. The reaction proceeds smoothly with diethyl dicarbonate in the presence of Mg(ClO4)2, a specific activator of 1,3-dicarbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::266eaf01e8e13d388231c808d30e4b7a
http://hdl.handle.net/11585/34867
http://hdl.handle.net/11585/34867
Autor:
MELCHIORRE, PAOLO, BARTOLI, GIUSEPPE, BOSCO, MARCELLA, CARLONE, ARMANDO, LOCATELLI, MANUELA, SAMBRI, LETIZIA
RISOLUZIONE CINETICA AMINOLITICA (AKR) DI EPOSSIDI TERMINALI: UN NUOVO STRUMENTO PER LA SINTESI DI IMPORTANTI MOLECOLE ENANTIOPURE P. Melchiorre, G. Bartoli, M. Bosco, A. Carlone, M. Locatelli, L. Sambri Dip. di Chimica Organica “A. Mangini” - Un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::f0dc1a347d39535b86c6cc5f6eaaa6a0
http://hdl.handle.net/11585/23074
http://hdl.handle.net/11585/23074