Journal article
A novel entry into the 6-azabicyclo[3.2.1]octane system via radical rearrangement of a tropane derivative
Tetrahedron letters, Vol.37(13), pp.2201-2204
1996
DOI: 10.1016/0040-4039(96)00259-6
Abstract
The conversion of an enantiomerically pure tropane derivative, obtained from chromium(0)-promoted [6
π + 2
π] cycloaddition, into a functionalized 6-azabicyclo[3.2.1]octane has been achieved
via a novel radical rearrangement process.
The conversion of an enantiomerically pure tropane derivative, obtained from chromium(0)-promoted [6
π+2
π] cycloaddition, into a functionalized 6-azabicyclo[3.2.1]octane has been achieved
via a novel radical rearrangement process.
Details
- Title: Subtitle
- A novel entry into the 6-azabicyclo[3.2.1]octane system via radical rearrangement of a tropane derivative
- Creators
- James H RigbyF.Christopher Pigge
- Resource Type
- Journal article
- Publication Details
- Tetrahedron letters, Vol.37(13), pp.2201-2204
- Publisher
- Elsevier Ltd
- DOI
- 10.1016/0040-4039(96)00259-6
- ISSN
- 0040-4039
- eISSN
- 1873-3581
- Language
- English
- Date published
- 1996
- Academic Unit
- Radiology; Chemistry
- Record Identifier
- 9984216569302771
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