PropertyValue
?:abstract
  • We have achieved a sequential hydride-shift-triggered double C(sp3)-H bond functionalization at a position adjacent to an oxygen atom and a benzylic/aliphatic position through the employment of substrates with a dialkyl group in the alkyl chain, which enabled the highly diastereoselective synthesis of fused tetrahydropyrans.
?:creator
?:doi
?:doi
  • 10.1021/acs.orglett.0c01867
?:journal
  • Organic_letters
?:license
  • cc-by-nc
?:pmid
?:pmid
  • 32667812.0
?:publication_isRelatedTo_Disease
?:source
  • Medline
?:title
  • Highly Stereoselective Synthesis of Fused Tetrahydropyrans via Lewis-Acid-Promoted Double C(sp3)-H Bond Functionalization.
?:type
?:year
  • 2020-07-15

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