ALBERT
GUIJARRO PASTOR
CATEDRATICO/A DE UNIVERSIDAD
MIGUEL ANGEL
YUS ASTIZ
Investigador en el periodo 1970-2018
Publicaciones en las que colabora con MIGUEL ANGEL YUS ASTIZ (29)
2012
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Concise total synthesis and stereochemical analysis of tetraponerines T3 and T4
Journal of Organic Chemistry, Vol. 77, Núm. 22, pp. 10340-10346
2011
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Isoprene-mediated lithiation of imidazole derivatives: Mechanistic considerations
Arkivoc, Vol. 2011, Núm. 5, pp. 12-22
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On the nature of lithium biphenyl in ethereal solvents. A critical analysis unifying DFT calculations, physicochemical data in solution, and a X-ray structure
Journal of Physical Chemistry B, Vol. 115, Núm. 49, pp. 14610-14616
2009
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Structural characterization and bonding properties of lithium naphthalene radical anion, [Li+(TMEDA)2][C10H8˙-], and lithium naphthalene dianion [(Li+TMEDA)2C10H8−2]
Journal of the Chemical Society. Dalton Transactions, pp. 1286-1289
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The reaction of biphenyl radical anion and dianion with alkyl fluorides. From ET to SN2 reaction pathways and synthetic applications
Tetrahedron, Vol. 65, Núm. 52, pp. 10769-10783
2007
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Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: New modes of reactivity of highly reduced organic species in solution
European Journal of Organic Chemistry, pp. 5514-5526
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New modes of reactivity in the threshold of the reduction potential in solution. alkylation of lithium PAH (Polycyclic Aromatic Hydrocarbon) dianions by primary fluoroalkanes: A reaction pathway complementing the classical birch reductive alkylation
Chemistry - A European Journal, Vol. 13, Núm. 36, pp. 10096-10107
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Reductive dearomatization of biphenyl: sequential one-pot regioselective introduction of two different electrophiles
Tetrahedron Letters, Vol. 48, Núm. 23, pp. 4105-4109
2006
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Reactivity in the upper limits of the reduction potential in solution: arene dianion intermolecular carbolithiation of alkenes
Tetrahedron Letters, Vol. 47, Núm. 35, pp. 6267-6271
2003
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Aliphatic organolithiums by fluorine-lithium exchange: n-octyllithium
Tetrahedron Letters, Vol. 44, Núm. 27, pp. 5025-5027
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On the dichotomy of the SN2/ET reaction pathways: An apparent SN2 reactivity in the reaction of naphthalene dianion with alkyl fluorides
Tetrahedron Letters, Vol. 44, Núm. 6, pp. 1309-1312
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Primary alkyl fluorides as regioselective alkylating reagents of lithium arene dianions. Easy prediction of regioselectivity by MO calculations on the dianion
Tetrahedron Letters, Vol. 44, Núm. 6, pp. 1313-1316
2002
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On the mechanism of arene-catalyzed lithiation: The role of arene dianions - Naphthalene radical anion versus naphthalene dianion
Chemistry - A European Journal, Vol. 8, Núm. 11, pp. 2574-2584
2001
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On the mechanism of the naphthalene-catalysed lithiation: The role of the naphthalene dianion
Tetrahedron Letters, Vol. 42, Núm. 20, pp. 3455-3458
1999
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N-(α-chloroalkyloxycarbonyl)pyrrolidines as a source of oxygenated d1- reagents
European Journal of Organic Chemistry, pp. 3005-3012
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α-Aminated methyllithium by DTBB-catalysed lithiation of a N- (chloromethyl) carbamate
Tetrahedron, Vol. 55, Núm. 15, pp. 4831-4842
1997
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Chiral lithiomethyl ethers by DTBB-catalyzed chlorine-lithium exchange
Anales de Quimica, Vol. 93, Núm. 1, pp. 44-48
1996
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Lithiomethyl ethyl ether from chloromethyl ethyl ether via a DTBB-catalysed lithiation
Tetrahedron, Vol. 52, Núm. 5, pp. 1643-1650
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N-(chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2- synthon
Tetrahedron Letters, Vol. 37, Núm. 31, pp. 5593-5596
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O-tert-butyl-N-(chloromethyl)-N-methyl carbamate as a source of the MeNHCH2- synthon
Tetrahedron Letters, Vol. 37, Núm. 31, pp. 5597-5600