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Double-bond geometries of 13 and 15 were confirmed by NOE measurements in comparison with their isomers.
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4 in PMB-OH, proceeded with moderate diastereoselectivity (de 79%) to mainly afford the (2R)-product, which can be attributed to the Si-face shielding by diethylphosphonodifluoromethyl group.
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Azide displacement of sultam-imide 34 gave much more amount of an E2-elimination product than that resulting from benzyl ester 35.
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4-benzyl alcohol in toluene at 120°C recovered the starting material. Furthermore, the reaction at elevated temperature gave decomposed products.
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