Derivation of elementary reaction about 82954-65-2

From this literature《Synthesis of phosphonoglycine backbone units for the development of phosphono peptide nucleic acids》,we know some information about this compound(82954-65-2)Product Details of 82954-65-2, but this is not all information, there are many literatures related to this compound(82954-65-2).

Product Details of 82954-65-2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (S)-(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine, is researched, Molecular C6H13NO2, CAS is 82954-65-2, about Synthesis of phosphonoglycine backbone units for the development of phosphono peptide nucleic acids. Author is Doboszewski, Bogdan; Groaz, Elisabetta; Herdewijn, Piet.

A series of phosphono-modified backbone mimics based on achiral and chiral N-(dihydroxypropyl)glycine units were obtained by sequential addition of phosphonate and nucleobase moieties to suitably protected dihydroxypropylamines. Simple synthetic strategies enabled the preparation of various target derivatives that will be useful as building blocks for the preparation of new synthetic polymers containing a phosphonate internucleotide linkage in place of the standard phosphodiester bond.

From this literature《Synthesis of phosphonoglycine backbone units for the development of phosphono peptide nucleic acids》,we know some information about this compound(82954-65-2)Product Details of 82954-65-2, but this is not all information, there are many literatures related to this compound(82954-65-2).

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics