Properties and Exciting Facts About 1,4,7,10,13,16-Hexaoxacyclooctadecane

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 17455-13-9. Category: chiral-catalyst.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 17455-13-9, Name is 1,4,7,10,13,16-Hexaoxacyclooctadecane, molecular formula is C12H24O6, belongs to chiral-catalyst compound. In a document, author is Kabes, Connor Q., introduce the new discover, Category: chiral-catalyst.

Tris(hydrochloride) adducts of the title compounds- are prepared from the inexpensive alpha-amino acids H2N(C=O)CH2CH(NH2)CO2H, HO(C=O)(CH2)(n ‘)CH(NH2)CO2H (n ‘ = 1, 2), and H2N(CH2)(4)CH(NH2)CO2H, respectively (steps/overall yield = 5/32%, 7/30%, 7/33%, 5/38%). The NH(2)group that is remote from the secondary amine is installed via BH(3)reduction of an amide [-(C=O)NR2] derived- from an alpha-amino carboxylic acid. The MeNHCH(2)units are introduced by BH(3)reductions of alkyl carbamate [RO(C=O)NHCH2-; R = Et,t-Bu] or amide [MeHN(C=O)-] moieties.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 17455-13-9. Category: chiral-catalyst.

Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare