406673-94-7Relevant academic research and scientific papers
Synthesis of the L-acid (C1-C18) fragment of pamamycin-593 and De-N-methylpamamycin-579
Miura, Ayako,Takigawa, Shin-Ya,Furuya, Yukito,Yokoo, Yusuke,Kuwahara, Shigefumi,Kiyota, Hiromasa
experimental part, p. 4955 - 4962 (2009/06/06)
The L-acid (C1-C18) fragment of pamamycin-593 and de-N-methylpamamycin-579, strong aerial mycelium-inducers of Streptomyces alboniger, was synthesized using a cis-selective iodoetherification and a nucleophilic addition of a cerium acetylide to an aldehyde as the key steps. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
Synthesis of southern (C1′-C11′) and eastern (C8-C18) fragments of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger
Kiyota, Hiromasa,Furuya, Yukito,Kuwahara, Shigefumi,Oritani, Takayuki
, p. 2630 - 2637 (2007/10/03)
Synthesis of the southern C1′-C11′ and eastern C8-C18 fragments of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger, was achieved. The southern fragment was synthesized by using the Evans aldol reaction and cis-selective iodoetherification as the key steps in a 9.6% overall yield (7 steps). The eastern fragment was constructed via the Julia coupling reaction and cis-selective iodoetherification in a 3.0% overall yield (8 steps from the known epoxide).
