Literature DB >> 10891165

Solid-phase peptide synthesis in the reverse (N --> C) direction.

N Thieriet1, F Guibé, F Albericio.   

Abstract

[reaction: see text] A new strategy for SPPS in the reverse direction based on the use of 2-Cl-trityl resin, an allyl ester as the temporary protecting group, and Cu(OBt)(2)/DIPCDI or HATU/DIEA as the coupling method is described. These conditions ensure good yields with minimal racemization of the C-terminal residue.

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Year:  2000        PMID: 10891165     DOI: 10.1021/ol0058341

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Sequence Diversification by Divergent C-Terminal Elongation of Peptides.

Authors:  Christine A Arbour; Ramona E Stamatin; Jennifer L Stockdill
Journal:  J Org Chem       Date:  2018-01-25       Impact factor: 4.354

Review 2.  Recent advances in the synthesis of C-terminally modified peptides.

Authors:  Christine A Arbour; Lawrence G Mendoza; Jennifer L Stockdill
Journal:  Org Biomol Chem       Date:  2020-09-30       Impact factor: 3.890

3.  Synthesis and characterization of a new Peptide prodrug of glucosamine with enhanced gut permeability.

Authors:  Hamed Gilzad Kohan; Kamaljit Kaur; Fakhreddin Jamali
Journal:  PLoS One       Date:  2015-05-15       Impact factor: 3.240

  3 in total

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