Zobrazeno 1 - 10
of 177
pro vyhledávání: '"José M. Saá"'
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
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0e92069455063b9134bdf6f1ce581fc
https://doi.org/10.1002/cphc.201901069
https://doi.org/10.1002/cphc.201901069
Autor:
Tito Arevalo-Ramirez, Anali Alfaro, Jose M. Saavedra, Matias Recabarren, Mauricio Ponce-Donoso, Jose Delpiano
Publikováno v:
IEEE Journal of Selected Topics in Applied Earth Observations and Remote Sensing, Vol 17, Pp 12112-12122 (2024)
Deep learning has gained popularity in recent years for reconstructing hyperspectral and multispectral images, offering cost-effective solutions and promising results. Research on hyperspectral image reconstruction feeds deep learning models with ima
Externí odkaz:
https://doaj.org/article/c3a65f46c9e8414aa60237fc9caddc56
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c1104753868ca62d9c43207428a4d87
https://doi.org/10.1002/chem.201604433
https://doi.org/10.1002/chem.201604433
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2490660a6e4dff365584761a94bd02f2
https://doi.org/10.1002/ange.201511555
https://doi.org/10.1002/ange.201511555
Autor:
Guido M. Rey Valzacchi, Diego Odetto, José M. Saadi, Liliana B. Zamora, Candela Loza, Milagros Medina, Myriam B. Perrotta
Publikováno v:
Gynecologic Oncology Reports, Vol 48, Iss , Pp 101226- (2023)
Objective: To report the surgical, oncological, and obstetrical outcomes of the different surgical techniques used for the fertility-sparing treatment of patients with early-stage cervical cancer. Methods: We retrospectively analyzed all fertility-sp
Externí odkaz:
https://doaj.org/article/d47e49030e604209a64fc2d8aeecd2d9
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7777490d51fa01e23ac6b1c9885e1b98
https://doi.org/10.1002/chin.201630199
https://doi.org/10.1002/chin.201630199
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af2009d3b60081c397dd52632bfd71a4
https://doi.org/10.1055/s-0029-1218751
https://doi.org/10.1055/s-0029-1218751
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630195118d4760caf7897a06aa120194
https://doi.org/10.1002/chir.20698
https://doi.org/10.1002/chir.20698