Stereoselectivity in the Wittig Reaction of Aromatic Ketones: Origin of Preference for the Olefin Geometry

DOI: 10.1021/jo00106a029

Source and publish data:

Journal of Organic Chemistry p. 156 - 168 (1995)

Update date:2022-08-03

Topics:

Authors:

Takeuchi, Kumiko

Paschal, Jonathan W.

Loncharich, Richard J.

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Article abstract of DOI:10.1021/jo00106a029

Investigation of the stereoselectivity observed in the Wittig reaction of aromatic ketones with "nonstabilized" phosphonium ylides revealed that the nature of the substituent on the phenyl ring of phenyl 3-pyridyl ketone determined the stereoselectivity.G

Full text of DOI:10.1021/jo00106a029

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