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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 19, 1989 - Issue 3-4
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Original Articles

Thiol Esters in Organic Synthesis. XV. Reduction with Tetrabutylammonium Borohydride

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Pages 387-392 | Received 20 Jun 1988, Published online: 23 Oct 2006

References

  • Liu , H. J. and Wynn , H. 1986 . Can. J. Chem. , 64 : 658 For part XIV of this series, see
  • Nagao , Y. , Kawabata , K. and Fujita , E. 1978 . Chem. Commun. , : 330
  • Liu , H. J. , Bukownik , R. R. and Pednekar , P. R. 1981 . Synth. Commun. , 11 : 599
  • Liu , H. J. and Wynn , H. 1982 . Tetrahedron Lett. , 23 : 3151
  • Liu , H. J. and Wynn , H. 1986 . Can. J. Chem. , 64 : 649
  • The thiol esters used for this investigation were readily obtained either by treatment of the acid chlorides with ethanethiol7 or directly from the carboxylic acids using phenyl dichlorophosphate as an activating agent.8
  • Liu , H. J. and Lai , H. K. 1979 . Can. J. Chem. , 57 : 2522
  • Liu , H. J. and Sabesan , S. I. 1980 . Can. J. Chem. , 23 : 2645

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