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- W3150802574 endingPage "1910" @default.
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- W3150802574 abstract "N-heteroaryl substituted adamantane-containing amines are of substantial interest for their perspective antiviral and psychotherapeutic activities. Chlorine atom at alpha-position of N-heterocycles has been substituted by the amino group using convenient nucleophilic substitution reactions with a series of adamantylalkylamines. The prototropic equilibrium in these compounds was studied using NMR spectroscopy. The introduction of the second amino substituent in 4-amino-6-chloropyrimidine, 2-amino-chloropyrazine, and 1-amino-3-chloroisoquinoline was achieved using Pd(0) catalysis." @default.
- W3150802574 created "2021-04-13" @default.
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- W3150802574 date "2021-03-29" @default.
- W3150802574 modified "2023-10-13" @default.
- W3150802574 title "Mono- and Diamination of 4,6-Dichloropyrimidine, 2,6-Dichloropyrazine and 1,3-Dichloroisoquinoline with Adamantane-Containing Amines" @default.
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- W3150802574 doi "https://doi.org/10.3390/molecules26071910" @default.
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