1,2-diacetals: a new opportunity for organic synthesis.
The use of 1,2-diacetals for a number of synthetic applications to provide diol protection and reactivity control was studied. The chiral versions of these systems were used to desymmetrize the enantiotopic diol pairs and to discriminate diequatorial diols in many carbohydrate derivatives. The fusio...
المؤلفون الرئيسيون: | Ley, S, Baeschlin, D, Dixon, D, Foster, A, Ince, S, Priepke, H, Reynolds, D |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
ACS
2001
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مواد مشابهة
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A general and efficient procedure for the preparation of enantiopure anti-1,2-diols - synthesis and utility of (R ',R ',S,R)-2,3-butane diacetal protected butane tetrol
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منشور في: (1999) -
Preparation of desymmetrised meso-tartrate derivatives - synthesis and utility of (R ',R ',R,S)-2,3-butane diacetal protected dimethyl tartrate
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The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol
حسب: Dixon, D, وآخرون
منشور في: (2001) -
Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids
حسب: Díez, E, وآخرون
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