Synthesis of configurationally chiral cryptands and cryptates from carbohydrate precursors
β Scribed by Curtis, W. David; Laidler, Dale A.; Stoddart, J. Fraser; Jones, Graham H.
- Book ID
- 120664775
- Publisher
- The Royal Society of Chemistry
- Year
- 1975
- Tongue
- English
- Weight
- 243 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-4936
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## 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 of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A six-step synthesis of racemic mycarose from allylacetylene is described. Key transformations include the &red-selective epoxidation of (E)-4-methyl-1,4heptadiend-ol and the a-opening of xylo-4,5-epoxy-4-methylhept-l-en-6-01 (7), which was accomplished via a neighboring group-assisted reaction of x
## 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.