1977
DOI: 10.1016/s0040-4039(01)92825-4
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Preparation of C-alkylated macrocyclic polyamines

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Cited by 136 publications
(45 citation statements)
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“…are in close agreement with their electronic spectral data, which further supports their proposed structure. [26][27][28][29] Bands due to zeolite encapsulated Cu(II) complex appeared in the visible, and charge transfer bands appeared in the near-UV region; these values were very similar to the obtained values for the discrete neat complex. [26][27][28][29] Several approaches have been used for the encapsulation of transition metal complexes in zeolite nanopores; 30 the choice of any specific method is dictated by the size of the ligand relative to the free diameter of the zeolite nanopores.…”
Section: Introductionsupporting
confidence: 75%
“…are in close agreement with their electronic spectral data, which further supports their proposed structure. [26][27][28][29] Bands due to zeolite encapsulated Cu(II) complex appeared in the visible, and charge transfer bands appeared in the near-UV region; these values were very similar to the obtained values for the discrete neat complex. [26][27][28][29] Several approaches have been used for the encapsulation of transition metal complexes in zeolite nanopores; 30 the choice of any specific method is dictated by the size of the ligand relative to the free diameter of the zeolite nanopores.…”
Section: Introductionsupporting
confidence: 75%
“…This is the "standard" procedure for preparing such C-alkylated macrocycles. 19 Reduction of the amide groups of dioxocyclam 2 using an excess of borane: methyl sulfide complex in THF did not furnish the desired anthrylmethylcyclam 3 cleanly.…”
Section: Syntheses Of Anthracenyl Cyclam Ligands and Complexesmentioning
confidence: 98%
“…Cyclization of these amines was carried out according to the method of Tabushi et al (13). Excess diethylmalonate was used and the unreacted ester was removed under high vacuum at room temperature.…”
Section: Cyclization Of LI and L2mentioning
confidence: 99%