Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde
The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were ela...
Ausführliche Beschreibung
Autor*in: |
Cheng, Xueli [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Schlagwörter: |
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Umfang: |
5 |
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Übergeordnetes Werk: |
Enthalten in: Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism - Lin, Heng ELSEVIER, 2016, New York, NY [u.a.] |
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Übergeordnetes Werk: |
volume:1113 ; year:2017 ; day:1 ; month:08 ; pages:105-109 ; extent:5 |
Links: |
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DOI / URN: |
10.1016/j.comptc.2017.05.013 |
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10.1016/j.comptc.2017.05.013 doi GBVA2017011000007.pica (DE-627)ELV040442586 (ELSEVIER)S2210-271X(17)30238-4 DE-627 ger DE-627 rakwb eng 540 540 DE-600 540 VZ 610 VZ 44.45 bkl Cheng, Xueli verfasserin aut Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde 2017 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. 8-exo-trig aldol Elsevier M06-2X Elsevier CH2 CHCHO Elsevier Aziridine aldehyde Elsevier Polycyclic compounds Elsevier Enthalten in Elsevier Lin, Heng ELSEVIER Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism 2016 New York, NY [u.a.] (DE-627)ELV019374771 volume:1113 year:2017 day:1 month:08 pages:105-109 extent:5 https://doi.org/10.1016/j.comptc.2017.05.013 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_70 44.45 Immunologie VZ AR 1113 2017 1 0801 105-109 5 045F 540 |
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10.1016/j.comptc.2017.05.013 doi GBVA2017011000007.pica (DE-627)ELV040442586 (ELSEVIER)S2210-271X(17)30238-4 DE-627 ger DE-627 rakwb eng 540 540 DE-600 540 VZ 610 VZ 44.45 bkl Cheng, Xueli verfasserin aut Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde 2017 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. 8-exo-trig aldol Elsevier M06-2X Elsevier CH2 CHCHO Elsevier Aziridine aldehyde Elsevier Polycyclic compounds Elsevier Enthalten in Elsevier Lin, Heng ELSEVIER Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism 2016 New York, NY [u.a.] (DE-627)ELV019374771 volume:1113 year:2017 day:1 month:08 pages:105-109 extent:5 https://doi.org/10.1016/j.comptc.2017.05.013 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_70 44.45 Immunologie VZ AR 1113 2017 1 0801 105-109 5 045F 540 |
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10.1016/j.comptc.2017.05.013 doi GBVA2017011000007.pica (DE-627)ELV040442586 (ELSEVIER)S2210-271X(17)30238-4 DE-627 ger DE-627 rakwb eng 540 540 DE-600 540 VZ 610 VZ 44.45 bkl Cheng, Xueli verfasserin aut Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde 2017 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. 8-exo-trig aldol Elsevier M06-2X Elsevier CH2 CHCHO Elsevier Aziridine aldehyde Elsevier Polycyclic compounds Elsevier Enthalten in Elsevier Lin, Heng ELSEVIER Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism 2016 New York, NY [u.a.] (DE-627)ELV019374771 volume:1113 year:2017 day:1 month:08 pages:105-109 extent:5 https://doi.org/10.1016/j.comptc.2017.05.013 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_70 44.45 Immunologie VZ AR 1113 2017 1 0801 105-109 5 045F 540 |
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10.1016/j.comptc.2017.05.013 doi GBVA2017011000007.pica (DE-627)ELV040442586 (ELSEVIER)S2210-271X(17)30238-4 DE-627 ger DE-627 rakwb eng 540 540 DE-600 540 VZ 610 VZ 44.45 bkl Cheng, Xueli verfasserin aut Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde 2017 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. 8-exo-trig aldol Elsevier M06-2X Elsevier CH2 CHCHO Elsevier Aziridine aldehyde Elsevier Polycyclic compounds Elsevier Enthalten in Elsevier Lin, Heng ELSEVIER Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism 2016 New York, NY [u.a.] (DE-627)ELV019374771 volume:1113 year:2017 day:1 month:08 pages:105-109 extent:5 https://doi.org/10.1016/j.comptc.2017.05.013 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_70 44.45 Immunologie VZ AR 1113 2017 1 0801 105-109 5 045F 540 |
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Enthalten in Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism New York, NY [u.a.] volume:1113 year:2017 day:1 month:08 pages:105-109 extent:5 |
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Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde |
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Electro-enhanced goethite activation of peroxydisulfate for the decolorization of Orange II at neutral pH: Efficiency, stability and mechanism |
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Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde |
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The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. |
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The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. |
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The intriguing dimerization mechanism of aziridine aldehyde free from any substituents and solvents, as well as the addition and cyclization mechanisms of its dimer with vinyl aldehyde in acetonitrile were investigated systematically, and the weak interactions among these amphoteric species were elaborated. |
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Cyclization mechanisms of the cyclic dimer of aziridine aldehyde with vinyl aldehyde |
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