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- W1965489301 abstract "Bringing closure: α-Imino esters that contain alkoxycarbonyl electron-withdrawing groups at the α-position of the imines are transformed into indolin-3-ones by a reductive cyclization by using bis(trimethylsilyl) aluminum chloride. The synthesis of trisubstituted tetrahydro-4-quinolones was also developed by a 1,3-aza-Brook rearrangement/Dieckmann condensation of α-imino esters with the lithium enolate of trimethylsilylacetate. LDA=lithium diisopropylamide; TMS=trimethylsilyl. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W1965489301 date "2013-01-17" @default.
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- W1965489301 title "Synthesis of Indolin-3-ones and Tetrahydro-4-quinolones from α-Imino Esters" @default.
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- W1965489301 doi "https://doi.org/10.1002/ajoc.201200174" @default.
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