Document Type

Article

Publication Date

1991

Abstract

Sažetak The question of the stability of the bicyclic form of AA is addressed by several theoretical methods varying in the level of sophistication. Both semi- empirical and ab initio approaches indicate that the bicyclic form is somewhat more stable than the 2,3-enediol tautomer (7). However, the tautomer I has a significantly higher dipole moment indicating that it gains additionally in stability if dissolved in polar solvents due to strong electrostatic solvent-solute interactions.

Source Citation

Hodošček, M.., Fodor, G.., & Eckert-Maksić, M.. (1991). Theoretical Study Of (3, 6) Cyclohemiketal Form Of L-Ascorbic Acid. Croatica Chemica Acta. Arhiv za Kemiju, 64(3), 529-537.

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