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- W2803430241 abstract "First total synthesis of carpatamide-A 7a, cytotoxic arylamine derivative isolated from marine derived Streptomyces sp., was achieved in twelve steps with overall yield of 24% with seven longest linear steps. In the penultimate step, dienoic acid 13 and an amino-phenylpropionic acid methyl ester core 21 were coupled to synthesize methylated derivativative of carpatamide-A 22 followed by demethylation of the intermediate with BBr3 to accomplish carpatamide-A 7a. Both precursors 13 and 21 were synthesized from readily available starting materials i.e. isovaleraldehyde 8 and 2, 4-dihydroxy benzaldehyde 14." @default.
- W2803430241 created "2018-06-01" @default.
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- W2803430241 date "2018-05-17" @default.
- W2803430241 modified "2023-10-14" @default.
- W2803430241 title "Convergent synthesis of Carpatamide-A: Cytotoxic arylamine derivative from marine derived <i>Streptomyces</i> sp." @default.
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- W2803430241 doi "https://doi.org/10.1080/14786419.2018.1460837" @default.
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