A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of (R)-2-Oxothiazolidine-4-carboxylic acid, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. Application In Synthesis of (R)-2-Oxothiazolidine-4-carboxylic acid, Name is (R)-2-Oxothiazolidine-4-carboxylic acid, molecular formula is C4H5NO3S. In a Patent, authors is ，once mentioned of Application In Synthesis of (R)-2-Oxothiazolidine-4-carboxylic acid
Thiazolidinone compounds and composition for angina pectoris comprising the compounds as an active ingredient
A thiazolidinone compound represented by general formula (I) or a pharmacoligically acceptable salt thereof, STR1 wherein W represents sulfur or oxygen and X represents –N(R1)–, or alternatively X represents sulfur or oxygen and W represents –N(R1)–, and R1 represents hydrogen, alkyl or substituted alkyl; R2 and R3 are the same or different from each other, and each represents hydrogen, alkyl, substituted alkyl, aryl, or 5- or 6-membered heteroaryl; R4 represents hydrogen, alkyl or substituted C1 -C4 alkyl; R5 represents substituted cycloalkyl which may contain nitrogen, provided the substituents include –B–ONO2 (wherein B represents a single bond or alkylene) as the indispensable member and alkyl groups as optional members; and A represents a single bond or alkylene, has an excellent anti-anginal effect and thus is useful as an angina pectoris remedy or preventive.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Application In Synthesis of (R)-2-Oxothiazolidine-4-carboxylic acid, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Application In Synthesis of (R)-2-Oxothiazolidine-4-carboxylic acid
Reference：
Quinuclidine – Wikipedia,
Quinuclidine | C7H639N | ChemSpider