Issue 18, 1971
From the journal:

Journal of the Chemical Society D: Chemical Communications

1,1,2-Trimethylpropyldialkylcyanoborates as intermediates for the synthesis of symmetrical, unsymmetrical, functionalised, and cyclic ketones

Andrew Pelter,   M. G. Hutchings  and  Keith Smith  

Abstract

The insertion reaction of cyanide into thexyldialkylcyanoborates, using acylation at low temperatures followed by oxidation, provides the mildest known method for the high-yield production of ketones from olefins via organoboranes.

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Article information

DOI
https://doi.org/10.1039/C2971001048B
Article type
Paper

J. Chem. Soc. D, 1971, 1048b-1050

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1,1,2-Trimethylpropyldialkylcyanoborates as intermediates for the synthesis of symmetrical, unsymmetrical, functionalised, and cyclic ketones

A. Pelter, M. G. Hutchings and K. Smith, J. Chem. Soc. D, 1971, 1048b DOI: 10.1039/C2971001048B

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