Ultrafast ring-opening reactions: a comparison of α-terpinene, α-phellandrene, and 7-dehydrocholesterol with 1,3-cyclohexadiene
✍ Scribed by Arruda, Brenden C.; Smith, Broc; Spears, Kenneth G.; Sension, Roseanne J.
- Book ID
- 120517950
- Publisher
- Royal Society of Chemistry
- Year
- 2013
- Tongue
- English
- Weight
- 353 KB
- Volume
- 163
- Category
- Article
- ISSN
- 1359-6640
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📜 SIMILAR VOLUMES
The regiosetective ring-opening reaction of a-methyl-B-propiolactone with 3,3-ethytenedioxybutytmagnesiwn bromide in the presence of copper(I) cataZyst afforded 2-methyl-6-oxoheptanoic acid, which was easily converted into IEI-3,7-dimethyl-2-octene-I,&dial in good yield.
## Abstract Ring‐opening polymerization of a new anhydro‐hexose monomer having an azido group, 1,6‐anhydro‐3‐azido‐2,4‐di‐__O__‐benzyl‐3‐deoxy‐β‐D‐allopyranose (A3ABA), was carried out with Lewis acid catalysts to give a stereoregular (1→6)‐α‐D‐allopyranan derivative having the azido group at the C