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- W2000873821 abstract "Homochiral 2-methylpyrrole derivatives are synthesized in high yields starting from chiral amino alcohols and 5-chloro-3-pentene-2-one. The photooxygenation of these compounds in the presence of a photosynthesizer furnishes the pyrrolooxazolone structures in high diastereoselectivities. In all of the examples, trans-isomers are formed as the major products." @default.
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- W2000873821 date "2004-01-01" @default.
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- W2000873821 title "Synthesis and photooxygenation of homochiral 2-methylpyrrole derivatives of chiral amino alcohols: simple, selective access to chiral bicyclic lactams" @default.
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- W2000873821 doi "https://doi.org/10.1016/j.tetasy.2003.11.011" @default.
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