The photosolvolysis of N-arylmethyladenines. Photoremovable N-arylmethyl protective groups for N-containing compounds
N-arylmethyladenines are photolyzed in water, giving adenine and the corresponding arylmethanols.The reaction is not only observed when the arylmethyl group is a metasubstituted benzyl, but also with more complex substituents like imidazopyridin-6-ylmethyl.Meta-substituted arylmethyl groups are proposed as photoremovable N-protective groups in adenine chemistry.
Er-Rhaimini, A.,Mohsinaly, N.,Mornet, R.
p. 5757 - 5760
(2007/10/02)
An improved procedure for the synthesis of 1-alkyladenines: removal of the ribofuranosyl group from 1-benzyl, 1-(3-methyl-2-butenyl)-, and 1-allyladenosine hydrobromide in acetic acid
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Itaya,Tanaka,Fujii,Leonard
p. 1449 - 1452
(2007/10/05)
THE SYNTHESIS OF COMPOUNDS POSSESSING KINETIN ACTIVITY. THE USE OF A
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LEONARD,FUJI
p. 73 - 75
(2007/10/04)
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