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References from Chiral Betti base immobilized on UiO-66-NH2: Synthesis and catalytic application in the asymmetric Henry reaction. Local targets link to admitted publications; unresolved targets remain external evidence.
Enantioselective catalysis with homochiral metal–organic frameworks
10.1039/b807083k · 2009 · External reference
Metal-organic frameworks in heterogeneous catalysis
2023 · External reference
Chiral metal–organic frameworks
10.1021/acs.chemrev.1c00740 · 2022 · External reference
A decade of UiO-66 research: a historic review of dynamic structure, synthesis mechanisms, and characterization techniques of an archetypal metal–organic framework
10.1021/acs.cgd.9b00955 · 2019 · External reference
NH2-modified UiO-66: structural characteristics and functional properties
10.3390/molecules28093916 · 2023 · External reference
Recent advances in the transformation reactions of the Betti base derivatives
10.1039/d4ra01256a · 2024 · External reference
A practical stereoselective synthesis of secondary and tertiary aminonaphthols: chiral ligands for enantioselective catalysts in the addition of diethylzinc to benzaldehyde
10.1016/s0957-4166(02)00651-1 · 2002 · External reference
Stereoselective synthesis of vicinal aminodiols, diamines and diaminols by the use of enantiopure aldehydes in the three-component aromatic Mannich-type reaction
10.1016/j.tetasy.2007.04.016 · 2007 · External reference
Acid-promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
10.1039/c0gc00013b · 2010 · External reference
Betti's base for crystallization-induced deracemization of substituted aldehydes: synthesis of enantiopure amorolfine and fenpropimorph
10.1039/c6ob02765b · 2017 · External reference
Synthesis and preliminary results on the catalytic activity of metal complexes obtained from C2‐symmetric ligands derived from R‐(+)‐Betti base
10.1002/slct.201600547 · 2016 · External reference
Application of chiral Betti base-copper complexes in enantioselective allylic oxidation of olefins, computational studies of the Betti bases, and docking of the resulting chiral allylic esters
2023 · External reference
Microwave-assisted, highly enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by chiral aminonaphthols
10.1016/j.tetasy.2008.01.025 · 2008 · External reference
Synthesis of (−)‐octalactin A by a strategic vanadium‐catalyzed oxidative kinetic resolution
10.1002/anie.200800554 · 2008 · External reference
Triarylborane ammonia complexes as ideal precursors for arylzinc reagents in asymmetric catalysis
10.1021/ol0515659 · 2005 · External reference
Catalytic asymmetric Henry reaction
10.1016/j.tetasy.2006.12.005 · 2006 · External reference
Advances in Henry reaction: a versatile method in organic synthesis
10.2174/1570193x16666190214150144 · 2020 · External reference
Catalytic enantioselective Henry reactions of isatins: application in the concise synthesis of (S)‐(−)‐spirobrassinin
10.1002/chem.201101025 · 2011 · External reference
Enantioselective synthesis of (R)-salmeterol employing an asymmetric Henry reaction as the key step
10.1016/j.tetasy.2011.08.008 · 2011 · External reference
Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions
10.1021/ja00037a068 · 1992 · External reference
Asymmetric nitroaldol reaction catalyzed by a chromium (III)–salen system
10.1016/j.tetasy.2007.10.023 · 2007 · External reference
Enantioselective Henry reaction catalyzed by optically active ketoiminatocobalt complexes
10.1246/cl.2004.614 · 2004 · External reference
Nanocrystalline MgO for asymmetric Henry and Michael reactions
10.1021/ja0440248 · 2005 · External reference
A dinuclear Zn catalyst for the asymmetric nitroaldol (Henry) reaction
10.1002/1521-3757(20020301)114:5<889::aid-ange889>3.0.co;2-8 · 2002 · External reference
A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction
10.1021/ja0373871 · 2003 · External reference
Catalytic asymmetric Henry reactions. A simple approach to optically active β-nitro α-hydroxy esters
10.1039/b105929g · 2001 · External reference
Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes
10.1039/b208859m · 2003 · External reference
Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes
10.1039/b613019d · 2007 · External reference
Asymmetric Henry reaction catalyzed by bifunctional copper‐based catalysts
10.1002/chir.20661 · 2009 · External reference
Synthesis of new planar chiral [2.2] paracyclophane schiff base ligands and their application in the asymmetric Henry reaction
10.1016/j.tetasy.2010.02.007 · 2010 · External reference
Enantioselective Henry reaction catalyzed with copper (II)–iminopyridine complexes
10.1016/j.tetasy.2007.06.023 · 2007 · External reference
Design of a chiral secondary amine ligand for copper-catalyzed anti-selective Henry reaction
10.1055/s-0034-1379607 · 2015 · External reference
Heterogeneous chiral copper complexes of amino alcohol for asymmetric nitroaldol reaction
10.1021/jo1010679 · 2010 · External reference
Chiral 1,1′-binaphthylazepine-derived amino alcohol catalyzed asymmetric Henry reaction
10.1016/j.tetasy.2011.01.026 · 2011 · External reference
A highly diastereo-and enantioselective copper (І)-catalyzed Henry reaction using a bis (sulfonamide)-diamine ligand
10.1021/jo101932a · 2011 · External reference
Formation of multi-stereogenic centers using a catalytic diastereoselective Henry reaction
10.1039/c0cc03022h · 2010 · External reference
Enantioselective Henry reaction catalyzed by Cu (II) salt and bipiperidine
10.1021/jo902664v · 2010 · External reference
Asymmetric benzoylation and Henry reaction using reusable polytopic bis (oxazoline) ligands and copper (II)
10.1039/c4nj00653d · 2014 · External reference
Functionalized magnetic nanoparticles as catalysts for enantioselective Henry reaction
10.1021/acsomega.9b02683 · 2019 · External reference
Heterogeneous asymmetric Henry reaction using a chiral bis (oxazoline)-copper complex immobilized on magnetically separable mesocellular mesoporous silica support
10.1016/j.tetasy.2010.01.024 · 2010 · External reference
Chiral amido-oxazoline functionalized MCM-41: a sustainable heterogeneous catalyst for enantioselective Kharasch–Sosnovsky and Henry reactions
10.1016/j.heliyon.2024.e39911 · 2024 · External reference
Copper complex of phenylglycine-functionalized UiO-66-NH2: a chiral MOF catalyst for enantioselective Henry reaction
10.1039/d4nj03149k · 2025 · External reference
Copper-catalyzed simultaneous dehydrogenation and enantioselective allylic oxidation of alkanes using chiral heterogeneous ligands to produce allylic esters and theoretical investigation of the mechanism
10.1002/aoc.7857 · 2025 · External reference
Synthesis and resolution of 1-(α-pyrrolidinylbenzyl)-2-naphthol and its application in the resolution of 2, 2′-dihydroxy-1, 1′-binaphthyl
10.1016/j.tetasy.2004.04.030 · 2004 · External reference
Novel preparation of non-racemic 1-[α-(1-azacycloalkyl) benzyl]-2-naphthols from Betti base and their application as chiral ligands in the asymmetric addition of diethylzinc to aryl aldehydes
10.1039/b204534f · 2002 · External reference
Revisiting the Betti synthesis: using a cheap, readily available, recyclable clay catalyst under solventless conditions
10.1002/ejoc.201800826 · 2018 · External reference
A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability
10.1021/ja8057953 · 2008 · External reference
Synthesis, characterization and catalytic activity of UiO-66-NH2 in the esterification of levulinic acid
10.3390/applnano2040025 · 2021 · External reference
Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity
10.1351/pac198557040603 · 1985 · External reference
Mesopore determination from nitrogen sorption isotherms: fundamentals, scope, limitations
1979 · External reference
Physisorption of gases, with special reference to the evaluation of surface area and pore size distribution (IUPAC Technical Report)
10.1515/pac-2014-1117 · 2015 · External reference
Catalytic allylic oxidation of alkenes using an asymmetric Kharasch–Sosnovsky reaction
10.1002/1521-3773(20011001)40:19<3567::aid-anie3567>3.0.co;2-c · 2001 · External reference
The henry (Nitroaldol) reaction
2014 · External reference
Copper-catalyzed enantioselective Henry reactions of α-keto esters: an easy entry to optically active β-nitro-α-hydroxy esters and β-amino-α-hydroxy esters
10.1021/jo025690z · 2002 · External reference
A dinuclear Zn catalyst for the asymmetric nitroaldol (Henry) reaction
10.1002/1521-3757(20020301)114:5<889::aid-ange889>3.0.co;2-8 · ExternalCitation · doi-reference
Catalytic allylic oxidation of alkenes using an asymmetric Kharasch–Sosnovsky reaction
10.1002/1521-3773(20011001)40:19<3567::aid-anie3567>3.0.co;2-c · ExternalCitation · doi-reference
Synthesis of (−)‐octalactin A by a strategic vanadium‐catalyzed oxidative kinetic resolution
10.1002/anie.200800554 · ExternalCitation · doi-reference
Copper-catalyzed simultaneous dehydrogenation and enantioselective allylic oxidation of alkanes using chiral heterogeneous ligands to produce allylic esters and theoretical investigation of the mechanism
10.1002/aoc.7857 · ExternalCitation · doi-reference
Catalytic enantioselective Henry reactions of isatins: application in the concise synthesis of (S)‐(−)‐spirobrassinin
10.1002/chem.201101025 · ExternalCitation · doi-reference
Asymmetric Henry reaction catalyzed by bifunctional copper‐based catalysts
10.1002/chir.20661 · ExternalCitation · doi-reference
Revisiting the Betti synthesis: using a cheap, readily available, recyclable clay catalyst under solventless conditions
10.1002/ejoc.201800826 · ExternalCitation · doi-reference
Synthesis and preliminary results on the catalytic activity of metal complexes obtained from C2‐symmetric ligands derived from R‐(+)‐Betti base
10.1002/slct.201600547 · ExternalCitation · doi-reference
Chiral amido-oxazoline functionalized MCM-41: a sustainable heterogeneous catalyst for enantioselective Kharasch–Sosnovsky and Henry reactions
10.1016/j.heliyon.2024.e39911 · ExternalCitation · doi-reference
Synthesis and resolution of 1-(α-pyrrolidinylbenzyl)-2-naphthol and its application in the resolution of 2, 2′-dihydroxy-1, 1′-binaphthyl
10.1016/j.tetasy.2004.04.030 · ExternalCitation · doi-reference
Catalytic asymmetric Henry reaction
10.1016/j.tetasy.2006.12.005 · ExternalCitation · doi-reference
Stereoselective synthesis of vicinal aminodiols, diamines and diaminols by the use of enantiopure aldehydes in the three-component aromatic Mannich-type reaction
10.1016/j.tetasy.2007.04.016 · ExternalCitation · doi-reference
Enantioselective Henry reaction catalyzed with copper (II)–iminopyridine complexes
10.1016/j.tetasy.2007.06.023 · ExternalCitation · doi-reference
Asymmetric nitroaldol reaction catalyzed by a chromium (III)–salen system
10.1016/j.tetasy.2007.10.023 · ExternalCitation · doi-reference
Microwave-assisted, highly enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by chiral aminonaphthols
10.1016/j.tetasy.2008.01.025 · ExternalCitation · doi-reference
Heterogeneous asymmetric Henry reaction using a chiral bis (oxazoline)-copper complex immobilized on magnetically separable mesocellular mesoporous silica support
10.1016/j.tetasy.2010.01.024 · ExternalCitation · doi-reference
Synthesis of new planar chiral [2.2] paracyclophane schiff base ligands and their application in the asymmetric Henry reaction
10.1016/j.tetasy.2010.02.007 · ExternalCitation · doi-reference
Chiral 1,1′-binaphthylazepine-derived amino alcohol catalyzed asymmetric Henry reaction
10.1016/j.tetasy.2011.01.026 · ExternalCitation · doi-reference
Enantioselective synthesis of (R)-salmeterol employing an asymmetric Henry reaction as the key step
10.1016/j.tetasy.2011.08.008 · ExternalCitation · doi-reference
A practical stereoselective synthesis of secondary and tertiary aminonaphthols: chiral ligands for enantioselective catalysts in the addition of diethylzinc to benzaldehyde
10.1016/s0957-4166(02)00651-1 · ExternalCitation · doi-reference
A decade of UiO-66 research: a historic review of dynamic structure, synthesis mechanisms, and characterization techniques of an archetypal metal–organic framework
10.1021/acs.cgd.9b00955 · ExternalCitation · doi-reference
Chiral metal–organic frameworks
10.1021/acs.chemrev.1c00740 · ExternalCitation · doi-reference
Functionalized magnetic nanoparticles as catalysts for enantioselective Henry reaction
10.1021/acsomega.9b02683 · ExternalCitation · doi-reference
Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions
10.1021/ja00037a068 · ExternalCitation · doi-reference
A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction
10.1021/ja0373871 · ExternalCitation · doi-reference
Nanocrystalline MgO for asymmetric Henry and Michael reactions
10.1021/ja0440248 · ExternalCitation · doi-reference
A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability
10.1021/ja8057953 · ExternalCitation · doi-reference
Copper-catalyzed enantioselective Henry reactions of α-keto esters: an easy entry to optically active β-nitro-α-hydroxy esters and β-amino-α-hydroxy esters
10.1021/jo025690z · ExternalCitation · doi-reference
Heterogeneous chiral copper complexes of amino alcohol for asymmetric nitroaldol reaction
10.1021/jo1010679 · ExternalCitation · doi-reference
A highly diastereo-and enantioselective copper (І)-catalyzed Henry reaction using a bis (sulfonamide)-diamine ligand
10.1021/jo101932a · ExternalCitation · doi-reference
Enantioselective Henry reaction catalyzed by Cu (II) salt and bipiperidine
10.1021/jo902664v · ExternalCitation · doi-reference
Triarylborane ammonia complexes as ideal precursors for arylzinc reagents in asymmetric catalysis
10.1021/ol0515659 · ExternalCitation · doi-reference
Catalytic asymmetric Henry reactions. A simple approach to optically active β-nitro α-hydroxy esters
10.1039/b105929g · ExternalCitation · doi-reference
Novel preparation of non-racemic 1-[α-(1-azacycloalkyl) benzyl]-2-naphthols from Betti base and their application as chiral ligands in the asymmetric addition of diethylzinc to aryl aldehydes
10.1039/b204534f · ExternalCitation · doi-reference
Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes
10.1039/b208859m · ExternalCitation · doi-reference
Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes
10.1039/b613019d · ExternalCitation · doi-reference
Enantioselective catalysis with homochiral metal–organic frameworks
10.1039/b807083k · ExternalCitation · doi-reference
Formation of multi-stereogenic centers using a catalytic diastereoselective Henry reaction
10.1039/c0cc03022h · ExternalCitation · doi-reference
Acid-promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
10.1039/c0gc00013b · ExternalCitation · doi-reference
Asymmetric benzoylation and Henry reaction using reusable polytopic bis (oxazoline) ligands and copper (II)
10.1039/c4nj00653d · ExternalCitation · doi-reference
Betti's base for crystallization-induced deracemization of substituted aldehydes: synthesis of enantiopure amorolfine and fenpropimorph
10.1039/c6ob02765b · ExternalCitation · doi-reference
Copper complex of phenylglycine-functionalized UiO-66-NH2: a chiral MOF catalyst for enantioselective Henry reaction
10.1039/d4nj03149k · ExternalCitation · doi-reference
Recent advances in the transformation reactions of the Betti base derivatives
10.1039/d4ra01256a · ExternalCitation · doi-reference
Design of a chiral secondary amine ligand for copper-catalyzed anti-selective Henry reaction
10.1055/s-0034-1379607 · ExternalCitation · doi-reference
Enantioselective Henry reaction catalyzed by optically active ketoiminatocobalt complexes
10.1246/cl.2004.614 · ExternalCitation · doi-reference
Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity
10.1351/pac198557040603 · ExternalCitation · doi-reference
Physisorption of gases, with special reference to the evaluation of surface area and pore size distribution (IUPAC Technical Report)
10.1515/pac-2014-1117 · ExternalCitation · doi-reference
Advances in Henry reaction: a versatile method in organic synthesis
10.2174/1570193x16666190214150144 · ExternalCitation · doi-reference
Synthesis, characterization and catalytic activity of UiO-66-NH2 in the esterification of levulinic acid
10.3390/applnano2040025 · ExternalCitation · doi-reference
NH2-modified UiO-66: structural characteristics and functional properties
10.3390/molecules28093916 · ExternalCitation · doi-reference
