A new application about (R)-Ethyl thiazolidine-4-carboxylate hydrochloride

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.COA of Formula: C6H12ClNO2S, you can also check out more blogs about86028-91-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.COA of Formula: C6H12ClNO2S, Name is (R)-Ethyl thiazolidine-4-carboxylate hydrochloride, molecular formula is C6H12ClNO2S, COA of Formula: C6H12ClNO2S. In a Article, authors is Zeidler, Juergen£¬once mentioned of COA of Formula: 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

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.COA of Formula: C6H12ClNO2S, you can also check out more blogs about86028-91-3

Reference£º
Quinuclidine – Wikipedia,
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