N-tert-butylbenzenesulfinimidoyl chloride

Product Manager：Nick Wilde

Recent Literature

A range of unsymmetrical ketones has been prepared in good yields from aldehydes in one simple synthetic operation by addition of organolithium compounds followed by an oxidation using N-tert-butylphenylsulfinimidoyl chloride.
J. J. Crawford, K. W. Hederson, W. J. Kerr, Org. Lett., 2006, 8, 5073-5076.

https://doi.org/10.1021/ol061903l

A one-pot procedure enables the conversion of various ketones into α,β-unsaturated ketones in very good yields under mild conditions via treatment of lithium enolates with N-tert-butyl phenylsulfinimidoyl chloride.
T. Mukaiyama, J.-i. Matsuo, H. Kitagawa, Chem. Lett., 2000, 1250-1251.

https://doi.org/10.1246/cl.2000.1250

Efficient carbon-carbon bond formation of N-carbobenzyloxy amines with 1,3-dicarbonyl compounds at the α-position of nitrogen was established by a one-pot oxidative Mannich reaction using N-tert-butylbenzenesulfinimidoyl chloride as an oxidant.
J-I. Matsuo, Y. Tanaki, H. Ishibashi, Org. Lett., 2006, 8, 4371-4374.

https://doi.org/10.1021/ol0618095

Quoted 

from:https://www.organic-chemistry.org/chemicals/oxidations/n-tert-butylbenzenesulfinimidoyl-chloride.shtm

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