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• W2068991024 abstract "A convenient preparation of (1R,2S,3R,4S)-3-(neopentyloxy)isoborneol (= (1R,2S,3R,4S)-3-(2,2-dimethyl-propoxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; 1a), a valuable chiral auxiliary, is described. The synthesis involves six steps starting from the readily available camphorquinone (5) and gives 1a in 48% overall yield. The key step is the chemoselective hydrolysis of the less hindered 1,3-dioxolane moiety in the camphorquinone di-acetal 4." @default.
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• W2068991024 date "1998-01-12" @default.
• W2068991024 modified "2023-10-15" @default.
• W2068991024 title "A Convenient Stereoselective Synthesis of (1<i>R</i>,2<i>S</i>,3<i>R</i>,4<i>S</i>)-3-(Neopentyloxy)isoborneol" @default.
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• W2068991024 doi "https://doi.org/10.1002/hlca.19980810109" @default.
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