An efficient protocol for chemoselective synthesis of previously unknown 1,4-benzodiazepin-2-ones and dienyl thiazolidin-4-one carboxylates in excellent yields by ring transformation reactions of functionally decorated 2-azetidin-3-thiazolidin-4-ones is reported.
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
SUGASAWA, T
ADACHI, M
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
ADACHI, M
SASAKURA, K
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
SASAKURA, K
MATSUSHITA, A
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
MATSUSHITA, A
EIGYO, M
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
EIGYO, M
SHIOMI, T
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
SHIOMI, T
SHINTAKU, H
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
SHINTAKU, H
TAKAHARA, Y
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN
TAKAHARA, Y
MURATA, S
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SHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPANSHIONOGI & CO LTD,SHIONOGI RES LAB,DIV NEUROPHARMACOL,FUKUSHIMA KU,OSAKA 553,JAPAN