A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of Methyl 1H-indole-5-carboxylate, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1011-65-0, Name is Methyl 1H-indole-5-carboxylate, molecular formula is C10H9NO2. In a Patent, authors is £¬once mentioned of 1011-65-0
FUSED HETEROCYCLIC RING COMPOUND
A compound represented by the following formula or a salt thereof, which has an GPR119 agonist action, is useful for the prophylaxis or treatment of diabetes, obesity and the like, and shows superior efficacy: wherein P: substituted 6-membered aromatic ring, Q: (substituted) 6-membered aromatic ring, A1: CR4aR4b, NR4c, O, S, SO or SO2 {R4a-4c: H etc.}, L1: (substituted) C1-5 alkylene, L2: a bond or (substituted) C1-3 alkylene, L3-4: (substituted) C1-3 alkylene, R1: H, X, CN, (substituted) hydrocarbon, (substituted) heterocycle or (substituted) OH, or (substituted) 4- to 8-membered (heterocyclic) ring together with A1, R2: H, CN, (substituted) hydrocarbon, and R3a: -COSRA1, (substituted) 5- or 6-membered aromatic ring {RA1: (substituted) hydrocarbon or (substituted) heterocycle}.
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 1011-65-0, help many people in the next few years.Application In Synthesis of Methyl 1H-indole-5-carboxylate
Reference£º
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles