5 years ago

Highly stereoselective construction of the C2 stereocentre of [small alpha]-tocopherol (vitamin E) by asymmetric addition of Grignard reagents to ketones

Highly stereoselective construction of the C2 stereocentre of [small alpha]-tocopherol (vitamin E) by asymmetric addition of Grignard reagents to ketones
Bartosz Bieszczad, Declan G. Gilheany
Both C2-diastereomers of [small alpha]-tocopherol can be prepared in three ways by asymmetric addition of Grignard reagents to ketones in up to 96 : 4 dr.

Publisher URL: http://feeds.rsc.org/~r/rss/OB/~3/_vOgo8ERJjI/C7OB00751E

DOI: 2017/OB/C7OB00751E

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