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. 61-76-7, Name is (R)-(-)-Phenylephrine hydrochloride, molecular formula is C9H14ClNO2. In an article, author is Bhattacharjee, Prantika,once mentioned of 61-76-7, Name: (R)-(-)-Phenylephrine hydrochloride.
Iodine-catalyzed selective C-3 benzylation of indoles with benzylic alcohols is developed. The reaction proceeds with molecular iodine as the catalyst under ligand-, metal-, and base-free conditions and tolerates wide functionalities. The experimental observations account for the halogenbond activation mechanistic pathway for the molecular iodine catalysis.
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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