The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Formula: C30H41FN4O12, 210344-95-9, Name is Z-DEVD-FMK, SMILES is O=C(N[C@@H](C(C)C)C(N[C@H](C(CF)=O)CC(OC)=O)=O)[C@H](CCC(OC)=O)NC([C@H](CC(OC)=O)NC(OCC1=CC=CC=C1)=O)=O, in an article , author is Yamamoto, Yuta, once mentioned of 210344-95-9.
One-Pot Heteroarene Synthesis Based on Ruthenium-on-Carbon-Catalyzed Oxidative Aromatization Using Oxygen
Various heteroarenes, such as indole, carbazole, dibenzofuran, dibenzothiophene, etc., were easily constructed by the Diels-Alder reaction of the corresponding vinyl-substituted pyrrole, indole, benzofuran or benzothiophene with the dienophiles and the subsequent heterogeneously ruthenium-on-carbon (Ru/C)-catalyzed oxidative aromatization using oxygen in a one-pot manner. Furthermore, the one-pot synthesis of the tetrahydropyrrolo[3,4-c]carbazole-1,3-dione derivative possessing the critical backbone of the antitumor agent was also accomplished by the following construction of the phthalimide moiety.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 210344-95-9, you can contact me at any time and look forward to more communication. Formula: C30H41FN4O12.
Reference:
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