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Search for "addition to α,β-unsaturated carbonyls" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.

A comprehensive review of flow chemistry techniques tailored to the flavours and fragrances industries

  • Guido Gambacorta,
  • James S. Sharley and
  • Ian R. Baxendale

Beilstein J. Org. Chem. 2021, 17, 1181–1312, doi:10.3762/bjoc.17.90

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Published 18 May 2021

Addition of dithi(ol)anylium tetrafluoroborates to α,β-unsaturated ketones

  • Yu-Chieh Huang,
  • An Nguyen,
  • Simone Gräßle,
  • Sylvia Vanderheiden,
  • Nicole Jung and
  • Stefan Bräse

Beilstein J. Org. Chem. 2018, 14, 515–522, doi:10.3762/bjoc.14.37

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  • dithiolanes by addition of an ynone to α-alkyl or aryl-substitued dithiolanylium TFBs. Keywords: addition to α,β-unsaturated carbonyls; dithiane chemistry; dithianylium tetrafluoroborate (TFB); ketene dithiane; Introduction 1,3-Dithioacetals are a common motif in organic chemistry. They are part of
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Published 26 Feb 2018

New approaches to organocatalysis based on C–H and C–X bonding for electrophilic substrate activation

  • Pavel Nagorny and
  • Zhankui Sun

Beilstein J. Org. Chem. 2016, 12, 2834–2848, doi:10.3762/bjoc.12.283

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  • -workers have re-evaluated the molecular iodine-catalyzed conjugate addition to α,β-unsaturated carbonyls or nitrostyrenes (Scheme 14) [80]. Based on their computational studies, they proposed that iodine activates the enone moiety by forming a halogen bond with the carbonyl and thus forming a more
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Published 23 Dec 2016
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