Reference of 95715-86-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 95715-86-9, Name is Methyl (R)-N-Boc-2,2-dimethyloxazolidine-4-carboxylate, molecular formula is C12H21NO5. In a Article£¬once mentioned of 95715-86-9
Multiple labeling of a potent CX3CR1 antagonist for the treatment of multiple sclerosis
Several methods for the preparation of five isotopologues of the CX 3CR1 antagonist 1 were developed. Volatile and radioactive 1-chloro- and 1-bromo-ethyl-benzene was handled in [2?-14C] and [3?, 5?-3H] labeling of 1. d-Leucinol ((R)-2-amino-4-methylpentan-1-ol) was labeled as [1-14C] and [4- 14C] via a Wittig reaction using Garner’s aldehyde and a Strecker amino acid synthesis with d-acylase resolvation, respectively. A [ 2H10]d-leucinol was used for the stable labeled [M + 10] isotopologue. The products were isolated with 97.6-100% stereo chemical and radiochemical purity as for specific activity 768 GBq/mmol and 1.6-2.0 GBq/mmol, respectively. Five isotopologues of the CX3CR1 antagonist 1 were developed. Volatile and radioactive 1-chloro- and 1-bromo-ethyl-benzene was handled in [2?-14C] and [3?, 5?-3H] labeling of 1. d-Leucinol was labeled as [1-14C] and [4- 14C] via a Wittig reaction using Garner’s aldehyde and a Strecker amino acid synthesis with d-acylase resolvation, respectively. A [ 2H10]d-leucinol was used for the stable labeled [M + 10] isotopologue. Copyright
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 95715-86-9. In my other articles, you can also check out more blogs about 95715-86-9
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2534NO – PubChem