1,2-Diacetals: A New Opportunity for Organic Synthesis
Chemical Reviews2000Vol. 101(1), pp. 53–80
Citations Over TimeTop 10% of 2000 papers
Steven V. Ley, Daniel K. Baeschlin, Darren J. Dixon, Alison C. Foster, Stuart J. Ince, Henning Priepke, Dominic J. Reynolds
Abstract
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 fusion of these rigid units to the carbohydrate substrates proved effective for tuning the reactivity during glycosidic coupling reactions. The studies confirmed that the methyl groups acted as useful diagnostic markers to analyze the nuclear magnetic resonance features of the compounds.
Related Papers
- → Basic Types of Correlation between Text and Icon, between Verbal and Visual Icons(2006)5 cited
- → Dietrich Icon , and: Josephine Baker in Art and Life: The Icon and the Image (review)(2009)1 cited
- → The Effect of Icon Prediction on College Students' Recall of Icon Codes(2000)
- Susquehanna Chorale Spring Concert "Roots and Wings"(2017)
- → Icon «The Judgment of the Jews over Christ» of the First Half of the XIX Century(2020)