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Acid stability of several benzylic protecting groups used in solid-phase peptide synthesis. Rearrangement of O-benzyltyrosine to 3-benzyltyrosine

✍ Scribed by Erickson, Bruce W.; Merrifield, R. B.


Book ID
111939108
Publisher
American Chemical Society
Year
1973
Tongue
English
Weight
938 KB
Volume
95
Category
Article
ISSN
0002-7863

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## Abstract The sequence‐dependent, acid‐ or base‐catalysed aspartimide formation is one of the most serious side reactions in solid‐phase synthesis of peptides containing aspartic acid. In the present work, we investigated the susceptibility of 4‐{__N__‐[1‐(4,4‐dimethyl‐2,6‐dioxocyclohexylidene)‐3