Synthesis of 13C- and 15N-labelled tert-butoxycarbonyl (boc) glycines and glycine amides as precursors and simple models of backbone-labelled peptides

Abstract
Boc-derivatives of the six 13C-labelled glycines with or without 15N have been prepared by a direct approach from the corresponding bromoacetates and three of them converted into 15N-labelled amides by an efficient procedure to give isotopomers with 2–4 adjacent 13C and 15N nuclei; their coupling constants have been recorded.

This publication has 0 references indexed in Scilit: