Literature DB >> 22236219

Mild reaction conditions for the terminal deuteration of alkynes.

Sean P Bew1, Glyn D Hiatt-Gipson, Jenny A Lovell, Christophe Poullain.   

Abstract

Routinely employed syntheses of terminally deuterated alkynes often utilize strong bases (i.e., LDA, n-BuLi, or Grignard reagents) or low (i.e., -78 °C) or elevated (i.e., 56 °C) reaction temperatures; furthermore many of these procedures afford average yields and in some cases less than optimum deuterium incorporation. Herein we report the application of alternative extremely mild reaction conditions that readily afford quantitative yields of terminally deuterated alkynes in a matter of minutes with exceptional isotope incorporation at ambient temperature.
© 2012 American Chemical Society

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Year:  2012        PMID: 22236219     DOI: 10.1021/ol2029178

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  7 in total

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2.  Synthesis of deuterated 1,2,3-triazoles.

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4.  Highly enantioselective copper-catalyzed propargylic amination to access N-tethered 1,6-enynes.

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5.  Why base-catalyzed isomerization of N-propargyl amides yields mostly allenamides rather than ynamides.

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6.  Solvent-Free Click-Mechanochemistry for the Preparation of Cancer Cell Targeting Graphene Oxide.

Authors:  Noelia Rubio; Kuo-Ching Mei; Rebecca Klippstein; Pedro M Costa; Naomi Hodgins; Julie Tzu-Wen Wang; Frederic Festy; Vincenzo Abbate; Robert C Hider; Ka Lung Andrew Chan; Khuloud T Al-Jamal
Journal:  ACS Appl Mater Interfaces       Date:  2015-08-20       Impact factor: 9.229

7.  Practical approaches to labelling terminal alkynes with deuterium.

Authors:  Melanie Y T Chan; Arbab Anwar; William J S Lockley
Journal:  J Labelled Comp Radiopharm       Date:  2022-02-02       Impact factor: 1.949

  7 in total

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