Abstract
Analysis of the contributions of 13C-1H dipolar interactions to the 13C n.m.r. spin-lattice relaxation times of the quaternary carbons of 1-methylisoguanosine establishes that the predominant tautomer in solution is the 2-keto, 6-amino form.
Original language | English |
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Pages (from-to) | 339-341 |
Number of pages | 3 |
Journal | Journal of the Chemical Society, Chemical Communications |
Issue number | 8 |
Publication status | Published - 1980 |
Externally published | Yes |