A synthesis of syributins 1 (5) and 2 (6) from D-glyceraldehyde acetonide (12) and furans (14) and (15) is described. Compounds (5) and (6) are cometabolites of the novel non-proteinaceous C-glycosidic elicitor molecules the syringolides 1 (1) and 2 (2). Under a variety of acidic conditions, the intermediate butenolides (9) and (10) provided syributins 1 (5) and 2 (6). Similar results have been reported by Honda and coworkers who converted butenolide (20) into syringolide 1 (1). Since compound (20) was also synthesized by the present new route, a formal synthesis of syringolide 1 (1) has been achieved.
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Mitsubishi Tanabe Pharma Co Ltd, Tianjin, Peoples R ChinaWaseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan
Utsugi, Masayuki
Iwamoto, Mitsuhiro
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Daiichi Sankyo Co Ltd, Tokyo, JapanWaseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan
Iwamoto, Mitsuhiro
Hirai, Sho
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Nippon Shinyaku Co Ltd, Kyoto, JapanWaseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan
Hirai, Sho
Kawada, Hatsuo
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Chugai Pharma Co Ltd, Tokyo, JapanWaseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan
Kawada, Hatsuo
Nakada, Masahisa
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Waseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, JapanWaseda Univ, Grad Sch Adv Sci & Engn, Dept Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan