Scytophysins are cytotoxic macrolides with a 22-membered ring and are characterized by their strong cytotoxicities targeting cytoskeletal protein actin. Toward the comprehensive total synthesis of scytophycins, we have investigated the late-state functionalization using fragment compounds. We established stereoselective construction of the C7-C21 part in scytophycins A and B involving characteristic C16 epoxide by using Sharpless epoxidation. Although stereoselectivity remains unsatisfactory, reduction of the C16 exo-olefin for the synthesis of scytophycin C was achieved.(c) 2022 Elsevier Ltd. All rights reserved.
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Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, JapanUniv Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
Kutsumura, Noriki
Numata, Keisuke
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Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, JapanUniv Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
Numata, Keisuke
Mosaki, Shiho
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Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, JapanUniv Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
Mosaki, Shiho
Saito, Takao
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Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, JapanUniv Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan