High anti Diastereoselectivity in a Tandem Oxyhomologation–Coupling Protocol for the Preparation of Amides and Peptides Incorporating α-Hydroxy β-Amino Acids
Author:
Affiliation:
1. Université Paris-Saclay, CNRS, ICMMO, 17 Avenue des Sciences, 91400 Orsay, France
Funder
Guangzhou Elite Project
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00370
Reference37 articles.
1. aChen, J.; Kuznetsova, L. V.; Ungreanu, I. M.; Ojima, I., in: Enantioselective Synthesis of β-Amino Acids, 2nd ed. Juaristi, E.; Soloshonok, V., Eds. Wiley: Hoboken, NJ, 2005; pp 447–476.
2. bSpiteller, P.; von Nussbaum, F. In Enantioselective Synthesis of β-Amino Acids, 2nd ed. Juaristi, E., Soloshonok, V., Eds. Wiley: Hoboken, NJ, 2005; pp 19–92.
3. Ziora, Z.; Skwarczynski, M.; Kiso, Y. In Amino Acids, Peptides and Proteins in Organic Chemistry, Vol. 4; Hughes, A. B., Ed. Wiley-VCH: Weinheim, 2011; pp 189–245.
4. Structure Revision of Microginins 674 and 690 from the Cultured Cyanobacterium Microcystis aeruginosa
5. Concise synthesis of AHMHA unit in perthamide C. Structural and stereochemical revision of perthamide C
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1. A Highly Diastereoselective Tandem Oxyhomologation–Coupling Method to Synthesize Amides and Peptides;Synfacts;2024-05-14
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