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Back Cover: A Convergent Strategy for the Synthesis of Type‐1 Elongated Mucin Cores 1–3 and the Corresponding Glycopeptides (Chem. Eur. J. 24/2014)
Author(s) -
Pett Christian,
Westerlind Ulrika
Publication year - 2014
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201490098
Subject(s) - glycopeptide , mucin , chemistry , disaccharide , acceptor , convergent synthesis , amino acid , sequence (biology) , stereochemistry , glycosylation , combinatorial chemistry , biochemistry , antibiotics , physics , condensed matter physics
Molecules singing in canon! In a convergent synthesis mode, by utilizing the differentiation in acceptor reactivity, shared early‐stage acceptor intermediates were elongated with a common type‐1 disaccharide donor. This resulted in an efficient synthesis of glycosylated amino acids carrying the type‐1 mucin core 1–3 saccharides. The obtained amino acids allowed for the preparation of different mucin core glycopeptides. For more information see the Full Paper by U. Westerlind and C. Pett on page 7287 ff.