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Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Safety of (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 Safety of (S)-4-Isopropylthiazolidine-2-thione

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Diastereoselective and Catalytic alpha-Alkylation of Chiral N-Acyl Thiazolidinethiones with Stable Carbocationic Salts

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, Safety of (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 Safety of (S)-4-Isopropylthiazolidine-2-thione

Reference£º
Quinuclidine – Wikipedia,
Quinuclidine | C7H734N | ChemSpider