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Photolysis of the 3,4-Epoxy-2-methyl-1-phenylbutan-1-ones and stereochemical assignment of the 3,4-Epoxy-2-methyl-1-phenylbutan-1-ols and 2-Methyl-1-phenylbut-3-en-1-ols

JM Coxon and GSC Hii
30(4) pp.835 - 842


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Diastereoselectivity, diastereofacial selectivity and regioselectivity in the reactions of cannamyl chloride with aldehydes mediated by tin and aluminium
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ChemInform Abstract: PHOTOLYSIS OF THE 3,4‐EPOXY‐2‐METHYL‐1‐PHENYLBUTAN‐1‐ONES AND STEREOCHEMICAL ASSIGNMENT OF THE 3,4‐EPOXY‐2‐METHYL‐1‐PHENYLBUTAN‐1‐OLS AND 2‐METHYL‐1‐PHENYLBUT‐3‐EN‐1‐OLS
COXON J. M., HII G. S. C.
Chemischer Informationsdienst. 1977 8(31).
On the Reaction Pathway and Stereochemistry of Allylic Tin Reagents-Benzaldehyde Condensation. A Substituent Effect Study
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Chemistry Letters. 1990 19(9). p.1711
The stereochemistry of the product homoallylic alcohols from a modified grignard reaction of 3-phenylpropen-1-yl chloride and benzaldehyde.
Coxon James M., Simpson Gregory W., Steel Peter J., Trenerry V.Craige
Tetrahedron Letters. 1983 24(13). p.1427

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