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Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH4 and CeCl37H 2O
Published in
2011
Volume: 41
   
Issue: 16
Pages: 2350 - 2358
Abstract
An efficient one-pot synthesis of α-hydroxy propargylic esters by chemoselective reduction followed by transesterification using NaBH4 in combination with CeCl37H2O is described. © 2011 Taylor & Francis Group, LLC.
About the journal
JournalSynthetic Communications
ISSN00397911
Open AccessNo
Concepts (12)
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    Cerium
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    Cerium chloride
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    Ester
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    Sodium borohydride
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    Unclassified drug
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    Article
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    Chemical reaction
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    CHEMOSELECTIVE REDUCTION
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    One pot synthesis
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    Reduction
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    Room temperature
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    Transesterification