Synthesis of protected ω-mercapto amino acids: precursors for incorporation of elongated cysteines into peptides
Authors:
- Joseph T. LundquistJLJoseph T. Lundquist
- Erika E. BüllesbachEBErika E. Büllesbach
- Thomas A. DixTDThomas A. Dix
- 1 August 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (15) , 2739-2743
Abstract
No abstract availableKeywords
Funding Information
- Medical University of South Carolina
This publication has 7 references indexed in Scilit:
- Asymmetric synthesis of ω-bromo-2(S)-azido acids as precursors for the synthesis of novel amino acidsTetrahedron Letters, 1998
- Conformational consequences of i, i + 3 cystine linkages: nucleation for α‐helicity?Chemical Biology & Drug Design, 1997
- Relative potencies of the somatostatin analogs octreotide, BIM-23014, and RC-160 on the inhibition of hormone release by cultured human endocrine tumor cells and normal rat anterior pituitary cells.Endocrinology, 1994
- General approach to the synthesis of short .alpha.-helical peptidesJournal of the American Chemical Society, 1991
- Rapid and efficient method for the preparation of Fmoc‐amino acids starting from 9‐fluorenylmethanolInternational Journal of Peptide and Protein Research, 1986
- Facile conversion of azides to aminesTetrahedron Letters, 1986
- Pyrylium-mediated transformations of natural products. Part 7. Displacement of the N-substituents of pyridinium ions in aqueous solution: replacement of the ω-amino group of lysine, and of the terminal amino group of glycylglycineJournal of the Chemical Society, Perkin Transactions 2, 1984