Reference of 100491-29-0, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 100491-29-0, Name is Ethyl 7-chloro-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate, molecular formula is C17H10ClF3N2O3. In a Article£¬once mentioned of 100491-29-0
N-Protected derivatives 12, 13 and 17 of 1alpha,5alpha,6beta-6-amino-3- azabicyclo[3.1.0]hexane 5 were synthesized via chloroenamines 6a or 6b. The specific N-protection was realized either by using a chloroenamine 6b with different protecting groups or by selective removal of identical protecting groups at the bicyclic target molecule 7. Dibenzylamino compound 13 allowed the preparation of naphthyridine derivative 25 which represents the 6beta- diastereomer of trovafloxacin mesylate, a potent Gyrase inhibitor.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 100491-29-0. In my other articles, you can also check out more blogs about 100491-29-0
Reference£º
1,803-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N797 – PubChem