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Because enzymes can increase reaction rates by enormous factors and tend to be very specific, name: (S)-4-Isopropylthiazolidine-2-thione, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about name: (S)-4-Isopropylthiazolidine-2-thione

New Advances in Chemical Research, May 2021. name: (S)-4-Isopropylthiazolidine-2-thione, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 76186-04-4, Name is (S)-4-Isopropylthiazolidine-2-thione, molecular formula is C6H11NS2. In a Article，once mentioned of 76186-04-4

Direct nickel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commercially available nickel(II) complex, (Me3P)2NiCl2, has been developed for tropylium and trityl tetrafluoroborate salts. The reaction provides a single diastereomer of the corresponding adducts in good to high yields, which, in turn, can be easily converted into a wide array of enantiomerically pure compounds that are difficult to obtain by other asymmetric procedures.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, name: (S)-4-Isopropylthiazolidine-2-thione, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about name: (S)-4-Isopropylthiazolidine-2-thione

Reference：
Quinuclidine – Wikipedia,
Quinuclidine | C7H734N | ChemSpider