Isopropylidenation of d-mannitol under neutral conditions
β Scribed by Gordon J.F. Chittenden
- Book ID
- 108308695
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 578 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0008-6215
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π SIMILAR VOLUMES
Recently, it was discovered['] that certain a-adamantyl car-bony1 compounds are considerably more active as antiviral agents and a great deal less toxic than 1 -aminoadamantane[2'. The multistep syntheses which were described in are based on phenols as starting materials, and are therefore restricte
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Primary and secondary alcohols are efficiently converted to the halides under neutral conditions.
The anomeric hydroxyl group of various furanose andpyranose hemiacetals can be replaced by a fluorine, chlorine, bromine or iodine atom under neutral conditions using haloenamines.