91287-28-4Relevant academic research and scientific papers
A novel and efficient method for cleavage of phenacylesters by magnesium reduction with acetic acid
Kokinaki, Stella,Leondiadis, Leondios,Ferderigos, Nikolas
, p. 1723 - 1724 (2007/10/03)
(Equation Presented) In the present study, we use magnesium turnings as a new deprotection reagent for the phenacyl group during orthogonal organic synthesis in the presence of other esters and sensitive protecting groups. By applying the new magnesium turnings/acetic acid deprotection method, phenacyl group can be more easily combined with other protecting groups that are not compatible with the zinc/acetic acid method.
Synthesis of α-aminophosphonic octapeptide, Phe-Gly-Ser-Leu-Ala(P)-Phl-Leu-Pro, an analog with partial sequence of erb B-2 gene product
Inami,Teshima,Miyashita,Shiba
, p. 942 - 949 (2007/10/02)
A chemical synthesis was performed of an octapeptide with a phosphonic ester linkage, which corresponds to a variation of the partial sequence of a gene product of erb B-2. The phosphonic ester linkage was successfully prepared through a coupling reaction
