Colorantes orgánicos para materiales fotónicos
COLORGANIC
Universidad Nacional de Educación a Distancia
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Universidad Nacional de Educación a Distancia (47)
2013
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Electron ionization-induced fragmentation of bridgehead-substituted norbornan-2-ones derived from fenchone
International Journal of Mass Spectrometry, Vol. 334, pp. 49-57
2012
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Water-trapping of unstable carbocations taking place into the inverted region of the Marcus equation. First experimental and computational evidence
Tetrahedron, Vol. 68, Núm. 13, pp. 2892-2898
2011
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Electron ionization mass spectral studies of bridgeheadsubstituted norbornan-2-ones: Camphor derivatives
Rapid Communications in Mass Spectrometry, Vol. 25, Núm. 3, pp. 395-409
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Stereoelectronic control in the solvolysis of spiroepoxidic 1-norbornyl triflates: Unexpected reactivity in 3-bromomethyl derivatives
Tetrahedron Letters, Vol. 52, Núm. 15, pp. 1762-1765
2010
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Unexpected reactivity of 10-hydroxycamphor under triflic anhydride treatment: Formation of a C
2
-pseudosymmetric camphorderived sulfite
Arkivoc, Vol. 2010, Núm. 3, pp. 15-22
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The role of the C(2) configuration and methyl substitution on the catalytic activity of novel 2,3,3- and 2,7,7-trimethyl-substituted γ- aminonorbornan-2-ols
Chirality, Vol. 22, Núm. 8, pp. 778-787
2008
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Solvent and stereoelectronic effects on the solvolysis rates of oxaspirocyclopropanated 1-norbornyl triflates and related bridgehead derivatives
Journal of Organic Chemistry, Vol. 73, Núm. 17, pp. 6607-6614
2007
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First efficient synthesis of enantiopure homoketopinic acid
Letters in Organic Chemistry, Vol. 4, Núm. 2, pp. 123-125
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The role of conformational flexibility on the catalytic activity of norbornane-derived β-, γ- and δ-amino alcohols
Tetrahedron Asymmetry, Vol. 18, Núm. 6, pp. 742-749
2005
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Enantiospecific access to 10-N-substituted camphors
Tetrahedron, Vol. 61, Núm. 3, pp. 599-601
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Understanding the catalytic role of flexible chiral δ-amino alcohols: The 1-(2-aminoethyl)norbornan-2-ol model
Tetrahedron, Vol. 61, Núm. 12, pp. 3055-3064
2004
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2-exo- versus 2-endo-Hydroxyl in δ-amino norbornan-2-ol-based catalysts: Investigating the role of the C(2) configuration in the asymmetric induction
Tetrahedron Asymmetry, Vol. 15, Núm. 5, pp. 753-756
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A short and convenient procedure for the stereoselective synthesis of 2-hydroxy-1-norbornanesulfonamides
Tetrahedron Asymmetry, Vol. 15, Núm. 2, pp. 293-298
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Enantiospecific access to various C(9),C(10)-disubstituted camphors: Scope and limitations
Journal of Organic Chemistry, Vol. 69, Núm. 21, pp. 7348-7351
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Intramolecular-activation evidence for the unexpected Beckmann fragmentation of C(1)-substituted-7-bromonorbornane-2-ones
Tetrahedron, Vol. 60, Núm. 42, pp. 9447-9451
2003
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C(10)-substituted camphors and fenchones by electrophilic treatment of 2-methylenenorbornan-1-ols: Enantiospecificity, scope, and limitations
Journal of Organic Chemistry, Vol. 68, Núm. 4, pp. 1451-1458
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First access to enantiopure C(7)-substituted fenchones: New norbornane-based chiral materials from the chiral pool
Tetrahedron Asymmetry, Vol. 14, Núm. 12, pp. 1607-1609
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Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Organic and Biomolecular Chemistry, Vol. 1, Núm. 4, pp. 700-704
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Synthesis and catalytic activity of 10-(aminomethyl)isoborneol-based catalysts: The role of the C(2)-group on the asymmetric induction
Tetrahedron Asymmetry, Vol. 14, Núm. 14, pp. 1959-1963
2002
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A new enantiospecific synthetic procedure to the taxoid-intermediate 10-methylenecamphor, and 10-methylenefenchone
Tetrahedron Asymmetry, Vol. 13, Núm. 1, pp. 17-19