A new synthetic route of 61302-99-6

When you point to this article, it is believed that you are also very interested in this compound(61302-99-6)Electric Literature of C4H11ClN2O and due to space limitations, I can only present the most important information.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: D-Alanine methylamide hydrochloride, is researched, Molecular C4H11ClN2O, CAS is 61302-99-6, about Peptide models for β-turns. A circular dichroism study.Electric Literature of C4H11ClN2O.

The CD spectra of β-turn model peptides PhCH2O2C-Aib-Pro-Aib-Pro-OMe (I, Aib = NHCMe2CO), Piv-Pro-Aib-NHMe (II, Piv = Me3CCO), Piv-Pro-D-Ala-NHMe (III), and Piv-Pro-Val-NHMe (IV) were examined in methanol, hexafluoroisopropanol, and cyclohexane. Type I and Type II β-turns were observed for I and II, resp., in the solid state, while the Pro-D-Ala sequence adopts a Type II β-turn in a related peptide crystal structure. A class C spectrum was observed for I in various solvents, suggesting a variant of a Type I (III) structure. The Type II β-turn is characterized by a CD spectrum having two pos. CD bands at ∼230 nm and ∼202 nm, a feature observed in III in cyclohexane and methanol and for II in methanol. II exhibits solvent-dependent CD spectra, which may be rationalized by considering Type II, III and V reverse turn structures. IV adopts non-β-turn structures in polar solvents, but exhibits a class B spectrum in cyclohexane suggesting a population of Type I β-turns.

When you point to this article, it is believed that you are also very interested in this compound(61302-99-6)Electric Literature of C4H11ClN2O and due to space limitations, I can only present the most important information.

Reference:
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem