Postsynthetic Modification of Peptides via Chemoselective N-Alkylation of Their Side Chains-Reference-Cited by-同舟云学术

Postsynthetic Modification of Peptides via Chemoselective N-Alkylation of Their Side Chains

Published:2012-03-12 Issue:7 Volume:14 Page:1664-1667
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Monfregola Luca¹,Leone Marilisa¹,Calce Enrica¹,De Luca Stefania¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States, and Institute of Biostructures and Bioimages, National Research Council, 80138 Naples, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol300437w

Reference18 articles.

1. Potent Human Immunodeficiency Virus Type 1 Protease Inhibitors That Utilize Noncoded d-Amino Acids as P2/P3 Ligands

2. N-Protected amino acid bromides: efficient reagents for the incorporation into peptides of extremely hindered α,α-dialkyl- and α-fluoroalkyl-amino acids

3. Amino Acid Bromides: Their N-Protection and Use in the Synthesis of Peptides with Extremely Difficult Sequences

4. Amino acid bromides: their utilization for difficult couplings in solid-phase peptide synthesis

5. Highly Stereoselective N-Terminal Functionalization of Small Peptides by Chiral Phase-Transfer Catalysis

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