NDLI: Biomimetic peptide bond formation in water with aminoacyl phosphate esters.

Content Provider	Semantic Scholar
Author	Dhiman, Raj S. Opiñska, Liliana Guevara Kluger, Ronald
Copyright Year	2011
Abstract	Aminoacyl phosphates, biomimetic analogues of aminoacyl adenylates, react efficiently with amino acid esters to form dipeptides with retention of stereochemical integrity. The reactions are selective and occur readily in the presence of nucleophiles other than amino groups on their side chains. Aminoacyl phosphate esters that lack an amino-protecting group are also suitable for peptide bond formation, leading to a simplified overall process.
Starting Page	89
Ending Page	92
Page Count	4
File Format	PDF HTM / HTML
Alternate Webpage(s)	http://www.rsc.org/suppdata/ob/c1/c1ob05660c/c1ob05660c.pdf
PubMed reference number	21735032v1
Alternate Webpage(s)	https://doi.org/10.1039/c1ob05660c
DOI	10.1039/c1ob05660c
Journal	Organic & biomolecular chemistry
Volume Number	9
Issue Number	16
Language	English
Access Restriction	Open
Subject Keyword	Amino Acids Amino Acyl-tRNA Synthetases Biomimetics Carbamoyl-Phosphate Synthase I Deficiency Disease Dipeptides Esters Phosphatidylinositol Phosphates Thioctic Acid inorganic phosphate
Content Type	Text
Resource Type	Article

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Biomimetic peptide bond formation in water with aminoacyl phosphate esters.