Chen, D.; Park, D.J.; Cadelis, M.M.; Douafer, H.; Bourguet-Kondracki, M.L.; Brunel, J.M.; Copp, B.R.
Total Synthesis of the Four Stereoisomers of Cyclo(l-Trp-l-Arg) Raises Uncertainty of the Structures of the Natural Products and Invalidates Their Promising Antimicrobial Activities. Molecules 2022, 27, 5913.
https://doi.org/10.3390/molecules27185913
AMA Style
Chen D, Park DJ, Cadelis MM, Douafer H, Bourguet-Kondracki ML, Brunel JM, Copp BR.
Total Synthesis of the Four Stereoisomers of Cyclo(l-Trp-l-Arg) Raises Uncertainty of the Structures of the Natural Products and Invalidates Their Promising Antimicrobial Activities. Molecules. 2022; 27(18):5913.
https://doi.org/10.3390/molecules27185913
Chicago/Turabian Style
Chen, Dan, Daniel J. Park, Melissa M. Cadelis, Hana Douafer, Marie Lise Bourguet-Kondracki, Jean Michel Brunel, and Brent R. Copp.
2022. "Total Synthesis of the Four Stereoisomers of Cyclo(l-Trp-l-Arg) Raises Uncertainty of the Structures of the Natural Products and Invalidates Their Promising Antimicrobial Activities" Molecules 27, no. 18: 5913.
https://doi.org/10.3390/molecules27185913
APA Style
Chen, D., Park, D. J., Cadelis, M. M., Douafer, H., Bourguet-Kondracki, M. L., Brunel, J. M., & Copp, B. R.
(2022). Total Synthesis of the Four Stereoisomers of Cyclo(l-Trp-l-Arg) Raises Uncertainty of the Structures of the Natural Products and Invalidates Their Promising Antimicrobial Activities. Molecules, 27(18), 5913.
https://doi.org/10.3390/molecules27185913