Solid phase reductive alkylation techniques in analogue peptide bond and sidechain modification
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (3) , 835-841
- https://doi.org/10.1016/s0040-4020(01)86120-2
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Solid-phase synthesis and biological properties of .psi.[CH2NH] pseudopeptide analogs of a highly potent somatostatin octapeptideJournal of Medicinal Chemistry, 1987
- Structure-activity studies of antagonists of luteinizing hormone-releasing hormone with emphasis on the amino-terminal regionJournal of Medicinal Chemistry, 1987
- Chemical modification of proteins: comments and perspectives*International Journal of Peptide and Protein Research, 1987
- Solid phase synthesis of peptides containing the CH2NH peptide bond isosterePeptides, 1987
- Synthesis and biological activities of some pseudo-peptide analogs of tetragastrin: the importance of the peptide backboneJournal of Medicinal Chemistry, 1985
- Hexapeptide analogue of somatostatin, Sandoz 201–456.International Journal of Peptide and Protein Research, 1985
- Conjugates of catecholamines. 1. N-Alkyl-functionalized carboxylic acid congeners and amides related to isoproterenolJournal of Medicinal Chemistry, 1983
- An Efficient Synthesis of Optically Active α-(t-Butoxycarbonylamino)-aldehydes from α-Amino AcidsSynthesis, 1983
- Potent new inhibitors of human reninNature, 1982
- Color test for detection of free terminal amino groups in the solid-phase synthesis of peptidesAnalytical Biochemistry, 1970