Studies on the Stereoselectivity of Hydride Reductions on 2-(Methylthio)- and 2-(Methylsulfonyl)cyclohexanones

DOI: 10.1021/jo00392a022

Source and publish data:

Journal of Organic Chemistry p. 3619 - 3625 (1987)

Update date:2022-07-31

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Authors:

Carreno, M. Carmen

Dominguez, Enrique

Garcia-Ruano, Jose L.

Rubio, Almudena

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Article abstract of DOI:10.1021/jo00392a022

The results obtained in the reductions of 2-X-cyclohexanones and cis- and trans-4-tert-butyl-2-X-cyclohexanones (X=SMe, SO2Me) with different hydrides are reported.When the sulfur functions adopt the axial disposition, the cyclohexanol resulting from the

Full text of DOI:10.1021/jo00392a022

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