Synthetic Route of 131833-93-7, 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. 131833-93-7, Name is (4S,4’S)-2,2′-(Propane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole), molecular formula is C17H30N2O2. In a Article£¬once mentioned of 131833-93-7
Concise total synthesis of albaflavenone utilizing sequential intramolecular aldol condensation: Determination of absolute configuration
The first total synthesis of albaflavenone, a novel antibiotic sesquiterpene, has been accomplished via the concise construction of its zizaene skeleton utilizing sequential intramolecular aldol condensation followed by chemo- and diastereoselective reduction of the conjugated carbon-carbon double bond. This synthetic work was completed in nine steps from 2-cyclopenten-1-one as a starting material without the use of protecting groups and with high stereocontrol. In addition, the absolute configuration of naturally occurring albaflavenone was determined to be 1R,2S and 8S.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 131833-93-7, you can also check out more blogs about131833-93-7
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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI