Zobrazeno 1 - 10
of 174
pro vyhledávání: '"José M. Saá"'
Autor:
Antonio Frontera, José M. Saá
Publikováno v:
ChemPhysChem. 21:313-320
In this manuscript we provide computational support to the catalytic role of water in all kinds of pseudopericyclic reactions operating in the reductive acid cycle, as well as in other metabolic processes. Water catalysis is not limited to those reac
Autor:
José M. Saá, Javier Mansilla
Publikováno v:
Molecules, Vol 15, Iss 2, Pp 709-734 (2010)
Conscious of the importance that stereochemical issues may have on the design of efficient organocatalyts for both Morita-Baylis-Hillman and aza-Morita-Baylis-Hillman reaction we have analyzed them in this minireview. The so-called standard reactions
Externí odkaz:
https://doaj.org/article/a2a711530ae548a9986d335679dafe74
Publikováno v:
Noncovalent Interactions in Catalysis ISBN: 9781788014687
The main paradigm of today's chemistry is sustainability. In pursuing sustainability, we need to learn from chemical processes carried out by Nature and realize that Nature does not use either strong acids, or strong bases or fancy reagents to achiev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70b77fe0446c6fb2fcae3ea579968845
https://doi.org/10.1039/9781788016490-00066
https://doi.org/10.1039/9781788016490-00066
Autor:
José M. Saá, Victor J. Lillo
Publikováno v:
Chemistry - A European Journal. 22:17182-17186
Organocatalysts displaying a network of cooperative hydrogen bonds (NCHB) have been employed in an enzyme-like manner for a direct, switchable synthesis of enantiopure hexahydropyrimidinones (HHPMs) or dihydropyrimidinones (DHPMs) which starts at a c
Publikováno v:
Angewandte Chemie. 128:4384-4388
The concept of noncovalent organocatalysis by means of networks of cooperative hydrogen bonds (NCHB organocatalysis) has been explored. Arylideneureas were chosen as ideal substrates because of their powerful donor-acceptor properties. We have examin
Publikováno v:
ChemInform. 47
The concept of noncovalent organocatalysis by means of networks of cooperative hydrogen bonds (NCHB organocatalysis) has been explored. Arylideneureas were chosen as ideal substrates because of their powerful donor-acceptor properties. We have examin
Publikováno v:
Synthesis. 2010:1909-1923
Enantiomerically enriched trifluoromethyl-substituted alcoholshaving a quaternary center of chirality can be prepared by the catalyticenantioselective addition of carbon nucleophiles to trifluoromethylketones, trifluoropyruvates, or the like. In part
Publikováno v:
Chirality. 21:836-842
Shelf stable, chiral-at-metal, D3 symmetric, 3:1 complexes of lanthanide (III) triflate salts are easily available by complexation with binolam (3,3′-diethylaminomethyl-2,2′-dihydroxy-1,1′-dinaphthalene) 1 or binolamo (3,3′-diethylaminooxymet
Publikováno v:
European Journal of Organic Chemistry. 2009:2385-2400
3,3'-Bis(dialkylaminomethyl)-1,1'-binaphth-2-ols (Binolams) have emerged during the last five years as very efficient chiral ligands in many enantioselective processes. Enantiomerically pure Binolams are easily accessible by means of a variety of met
Autor:
José M. Saá, Manuel Yáñez
Publikováno v:
Chemistry - A European Journal. 15:3123-3129
Predictions (DFT/B3LYP calculations) are that cyclopentadienyl lithium edge-fused to [n]circulenes in a circum-like manner should self-assemble as rod-like, nanometer long, supersandwich compounds (see figure). On the contrary, triazolyl lithium anal