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- W2952600458 abstract "Abstract The unusual natural amino acid 3,4-didehydro-5-phosphono-D-norvaline, D4, and the cyclic analogue 14 have been synthesized by four- and three-component condensation of the aldehydes 3 and 10 , respectively. Strict selectivity has been observed in the enzyme-substrate interactions with the enzymes phosphodiesterase I, alkaline phosphatase, α-chymotrypsin, urease, and alkaline mesintericopeptidase. The tripeptide antibiotics Plumbemicin A, 21 , and B, 25 , have been synthesized by the methods of conventional peptide synthesis and enzyme-catalyzed removal of the protective groups. Biological tests of the newly synthesized compounds have shown that they possess herbicidal, fungicidal, and antitumour activity." @default.
- W2952600458 created "2019-06-27" @default.
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- W2952600458 date "1988-07-19" @default.
- W2952600458 modified "2023-09-25" @default.
- W2952600458 title "ChemInform Abstract: Total Synthesis, Enzyme-Substrate Interactions and Herbicidal Activity of Plumbemicin A and B (N-1409)." @default.
- W2952600458 cites W2044488075 @default.
- W2952600458 doi "https://doi.org/10.1002/chin.198829296" @default.
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