Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Victor J. Lillo"'
Publikováno v:
ARKIVOC, Vol 2010, Iss 3, Pp 29-44 (2009)
Externí odkaz:
https://doaj.org/article/dadbd6cf2af64a0e95df2ce278c00339
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
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:
Tetrahedron Letters. 50:2266-2269
The reaction of biphenylene ( 1 ) with an excess of lithium powder (1:14 molar ratio) and a catalytic amount of DTBB (10 mol %) in THF at room temperature leads to the formation of the dilithiated species I by reductive opening of the four-membered r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a56ed20b254922e7567b316ef6205acc
https://doi.org/10.1016/j.tetlet.2009.02.216
https://doi.org/10.1016/j.tetlet.2009.02.216
Publikováno v:
ARKIVOC, Vol 2010, Iss 3, Pp 29-44 (2009)
The reaction of cyclopropylidene diphenylmethane 1 with an excess of lithium and a catalytic amount of naphthalene (5 mol %) at -20 oC, followed by addition of an electrophile [E = H2O, D2O, t-BuCHO, Me2CO, Et2CO, n-Pr2CO, i-Pr2CO, (c-C3H5)2CO, (CH2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62a5757fd4dcdcbb6e91e0b5cb869e7e
https://doi.org/10.3998/ark.5550190.0011.305
https://doi.org/10.3998/ark.5550190.0011.305
Publikováno v:
Tetrahedron Letters. 49:5182-5185
The reaction of 2,2-diphenylmethylenecyclopropane (5) with an excess of lithium and a catalytic amount of DTBB (4 mol %) in THF at −78 °C leads to the formation of dilithiated species 6–8 by reductive opening of the cyclopropane ring. Further re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75a79a49bd27c553d28cbcab890e507b
https://doi.org/10.1016/j.tetlet.2008.06.065
https://doi.org/10.1016/j.tetlet.2008.06.065
Publikováno v:
Synthesis. 2008:1241-1248
The reaction of acenaphthylene with an excess of lithium powder and a catalytic amount of DTBB (7.5 mol%) in tetrahydrofuran at -70 °C followed by treatment with a carbonyl compound [Me 2 CO, Et 2 CO, I-Pr 2 CO, ( C-C 3 H 5 ) 2 CO, cyclopentanone, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09ca84877a18f2efc7fcb1107493ff4f
https://doi.org/10.1055/s-2008-1042943
https://doi.org/10.1055/s-2008-1042943