One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of (R)-Ethyl thiazolidine-4-carboxylate hydrochloride, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 86028-91-3, Name is (R)-Ethyl thiazolidine-4-carboxylate hydrochloride, molecular formula is C6H12ClNO2S
Synthesis of heterocyclic platelet activating factor analogues
The synthesis of heterocyclic analogues of the platelet activating factor is described.The preparation starts with acylating rac-tetrahydro-1,3-thiazine-4-carboxylic acid ethyl ester, with palmitoyl chloride to form the amide linkage.Following ester reduction, the phosphocholine part is introduced via 2-chloro-2-oxo-1,3,2-dioxaphospholane and subsequent ring opening with trimethylamine under pressure.Furthermore, the related L-thiazolidine analogue is prepared using the same procedure.In addition the sulfinyl and sulfonyl derivatives of this compound are obtained by oxidation with 3-chloro-perbenzoic acid.From one sulfinyl intermediate the diastereomeres are separated and their conformations are determined by 13C-NMR spectroscopy. Keywords: Phospholipid synthesis; Cyclic platelet activating factor analogue; Cyclic thioether; Chiral sulphur compound
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of (R)-Ethyl thiazolidine-4-carboxylate hydrochloride, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 86028-91-3, in my other articles.
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Quinuclidine – Wikipedia,
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