An Epoxide Rearrangement -Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue. -Base-promoted isomerization of the epoxide (I) provides the azanortricyclanol (II). The latter can be readily converted to the derivatives (V) as precurso
ChemInform Abstract: An Unusual Oxidative Rearrangement of Azabicyclo[2.2.1]heptenes, Providing a Stereoselective Route to 2′- and 3′-Hydroxycyclopentylglycines.
✍ Scribed by Patrick D. Bailey; I. M. McDonald; Georgina M. Rosair; David Taylor
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 30 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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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 “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v