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.
Digital Commons Citation
Hodošček, M.; Fodor, G.; and Eckert-Maksić, M., "Theoretical Study of (3, 6) Cyclohemiketal Form of L-Ascorbic Acid" (1991). Faculty & Staff Scholarship. 390.
https://researchrepository.wvu.edu/faculty_publications/390
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.