Studies in tautomerism new generalizations on o-benzoibenzoic acids
β Scribed by M.V. Bhatt; K.M. Kamath
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- French
- Weight
- 221 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The four most important tautomers of the title compound were studied by the ab initio LCAO-MO method at the MP2/ 6-31G\*\*//HF/3-21G level. All calculated structures are minima at the HF/3-2 1G potential energy surface with the dioxo tautomer 1 being the global minimum. 41~0 in a polar environment 1
## Abstract The inhibitive effect of some amino acids, glycine (Gly), alanine (Ala), valine (Val), leucine (Leu), isoleucine (Ile), serine (Ser), threonine (Thr), methionine (Met), phenylalanine (Phe), tyrosine (Tyr), trytophan (Try), aspartic acid (Asp), asparagine (Asn), glutamic acid (Glu), and
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