Search Results - "Natsume, Satomi"

Novel Azalides Derived from Sixteen-Membered Macrolides: I. Isolation of the Mobile Dialdehyde and Its One-Pot Macrocyclization with an Amine by Miura, Tomoaki, Natsume, Satomi, Kanemoto, Kenichi, Atsumi, Kunio, Fushimi, Hideki, Sasai, Hiroaki, Arai, Takayoshi, Yoshida, Takuji, Ajito, Keiichi

“…The design and synthesis of novel 15-membered 11-azalides and 16-membered 11,12-diazalide starting from 16-membered macrolides are reported. A mobile linear…”
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Novel azalides derived from 16-membered macrolides. III. Azalides modified at the C-15 and 4″ positions: Improved antibacterial activities by Miura, Tomoaki, Natsume, Satomi, Kanemoto, Kenichi, Shitara, Eiki, Fushimi, Hideki, Yoshida, Takuji, Ajito, Keiichi

“…The design and synthesis of 16-membered azalides modified at the C-15 and 4″ positions are described. 3-Hydroxyl azalides having an arylpropenyl and an…”
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Novel azalides derived from 16-membered macrolides. Part II: Isolation of the linear 9-formylcarboxylic acid and its sequential macrocyclization with an amino alcohol or an azidoamine by Miura, Tomoaki, Kanemoto, Kenichi, Natsume, Satomi, Atsumi, Kunio, Fushimi, Hideki, Yoshida, Takuji, Ajito, Keiichi

“…The design and synthesis of novel 14- to 16-membered 11-azalides and 11-azalactams starting from 16-membered macrolides are described. Fifteen-substituted…”
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Novel Azalides Derived from Sixteen-Membered Macrolides by Miura, Tomoaki, Natsume, Satomi, Kanemoto, Kenichi, Atsumi, Kunio, Fushimi, Hideki, Sasai, Hiroaki, Arai, Takayoshi, Yoshida, Takuji, Ajito, Keiichi

“…The design and synthesis of novel 15-membered 11-azalides and 16-membered 11,12-diazalide starting from 16-membered macrolides are reported. A mobile linear…”
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