Extended knowledge of (S)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl

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.Electric Literature of 100165-88-6, you can also check out more blogs about100165-88-6

Electric Literature of 100165-88-6, 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. 100165-88-6, Name is (S)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl, molecular formula is C48H40P2. In a Article£¬once mentioned of 100165-88-6

Catalytic Hydrothiolation: Regio- and Enantioselective Coupling of Thiols and Dienes

We report a Rh-catalyzed hydrothiolation of 1,3-dienes, including petroleum feedstocks. Either secondary or tertiary allylic sulfides can be generated from the selective addition of a thiol to the more substituted double bond of a diene. The catalyst tolerates a wide range of functional groups, and the loading can be as low as 0.1 mol %.

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.Electric Literature of 100165-88-6, you can also check out more blogs about100165-88-6

Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI