Amino Acid Bromides: Their N-Protection and Use in the Synthesis of Peptides with Extremely Difficult Sequences-Reference-Cited by-同舟云学术

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

Published:2002-08-14 Issue:18 Volume:67 Page:6372-6375
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

DalPozzo Alma¹,Ni Minghong¹,Muzi Laura¹,Caporale Andrea¹,de Castiglione Roberto¹,Kaptein Bernard¹,Broxterman Quirinus B.¹,Formaggio Fernando¹

Affiliation:

1. G. Ronzoni Institute for Chemical and Biochemical Research, via G. Colombo 81, 20133 Milano, Italy, Department of Fine Chemicals, Advanced Synthesis and Catalysis, DSM Research, P.O. Box 18, 6160 MD Geleen, The Netherlands, and Department of Organic Chemistry, University of Padova, Institute of Biomolecular Chemistry, CNR, 35131 Padova, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo020280w

Reference16 articles.

1. Koksch, B.; Sewald, N.; Jakubke, H.D.; Burger, K. InBiochemicalFrontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Symposium Series 639; American Chemical Society: Washington, DC, 1996; pp 42−58.

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. Peptide Synthesis via Amino Acid Halides

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