Synthesis of N-Fmoc-(2S,3S,4R)-3,4-dimethylglutamine: An Application of Lanthanide-Catalyzed Transamidation
Author:
Affiliation:
1. Department of Chemistry and Cancer Center, Purdue University, 560 Oval Drive, West Lafayette, Indiana 47907-2084
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo050518r
Reference12 articles.
1. Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.
2. Papuamides A−D, HIV-Inhibitory and Cytotoxic Depsipeptides from the Sponges Theonella mirabilis and Theonella swinhoei Collected in Papua New Guinea
3. Progress toward the Total Synthesis of Callipeltin A (I): Asymmetric Synthesis of (3S,4R)-3,4-Dimethylglutamine
4. Stereoselective synthesis of (3S,4R)-3,4-dimethyl-(S)-glutamine and the absolute stereochemistry of the natural product from papuamides and callipeltin
5. Synthesis and analysis of the sterically constrained l-glutamine analogues (3S,4R)-3,4-dimethyl-l-glutamine and (3S,4R)-3,4-dimethyl-l-pyroglutamic acid
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