Efficient total syntheses of the oligopeptide antibiotics netropsin and distamycin
JW Lown, K Krowicki
Index: Lown, J. William; Krowicki, Krzysztof Journal of Organic Chemistry, 1985 , vol. 50, # 20 p. 3774 - 3779
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Citation Number: 106
Abstract
New and efficient total syntheses of the natural oligopeptide antiviral antibiotics netropsin and distamycin are described. These procedures feature a different strategy of introduction of the terminal groups from that used hitherto, high yield coupling steps, improvements in the Pinner reaction for introducing the amidine moiety, and the novel use of N-formylimidazole for introduction of the formyl moiety in distamycin. The methods also avoid column ...
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