A modified backbone amide linker (BAL) solid-phase peptide synthesis strategy accommodating prolyl, N-alkylamino acyl, or histidyl derivatives at the C-terminus
- 1 September 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (38) , 7277-7280
- https://doi.org/10.1016/s0040-4039(00)01255-7
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides1,2,3Journal of the American Chemical Society, 1998
- PyBOP®: A new peptide coupling reagent devoid of toxic by-productTetrahedron Letters, 1990
- Protection of histidine in peptide synthesis: A Reassessment of the trityl groupTetrahedron Letters, 1987
- Racemisation of activated, urethane-protected amino-acids by p-dimethyl-aminopyridine. Significance in solid-phase peptide synthesisJournal of the Chemical Society, Chemical Communications, 1981