Chemical Research Letters, May 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction.Safety of 2-(5-Bromo-2-fluorobenzyl)benzo[b]thiophene, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1034305-17-3, Name is 2-(5-Bromo-2-fluorobenzyl)benzo[b]thiophene, molecular formula is C15H10BrFS
A concise and practical stereoselective synthesis of ipragliflozin L-proline was presented starting from 2-[(5-iodo-2-fluorophenyl)methyl]-1-benzothiophene and 2,3,4,6-tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide without catalyst via iodine?lithium?zinc exchange. The overall yield was 52% in three steps and the product purity was excellent. Two key diastereomers were prepared with efficient and direct access to the alpha-C-arylglucoside.
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Reference：
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem