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note
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Initially, the assembly by a simple amide formation between an α,β-unsaturated carboxylic acid derivative of adenosine moiety and the aniline 8 was attempted to prepare the precursor 15. However, these efforts were failed to occur, and only a trace amount of 15 was obtained presumably because of the low reactivity of either the carboxylic acid derivative or 8.
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67650388058
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note
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1H NMR and MS analyses indicated that the mixture contained several C-2 symmetric cyclic dimers including head-to-head and head-to tail ones.
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46
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23644441141
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Synthesis of a similar compound has been reported.
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Synthesis of a similar compound has been reported. Hanessian S., Huang G., Chenel C., Machaalani R., and Loiseleur O. J. Org. Chem. 70 (2005) 6721-6734
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67650436455
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note
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One of the atropisomers was used. It was confirmed that the use of the other atropisomer also gave the similar results to afford trans-4.
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50
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67650412738
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note
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Biological activity of cis- and trans-4 was briefly examined, however none of them showed cytotoxicity against human breast cancer SKBr-4 cells.
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