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Synthetic Application of Intramolecular Cyanoboration on the Basis of Removal and Conversion of a Tethering Group by Palladium-Catalyzed Retro-Allylation
- Source :
- Synlett. 2008:423-427
- Publication Year :
- 2008
- Publisher :
- Georg Thieme Verlag KG, 2008.
-
Abstract
- A new synthetic strategy, involving utilization of a tethered intramolecular reaction with a removable tether, was demonstrated by the intramolecular cyanoboration-retro-allylation sequence.
- Subjects :
- endocrine system
alkenes
Intramolecular reaction
Chemistry
Stereochemistry
Tethering
organic chemicals
Organic Chemistry
food and beverages
chemistry.chemical_element
Sequence (biology)
palladium
Combinatorial chemistry
Catalysis
nitrites
retro-allylation
Intramolecular force
nitriles
arylation
Palladium
Subjects
Details
- ISSN :
- 14372096 and 09365214
- Volume :
- 2008
- Database :
- OpenAIRE
- Journal :
- Synlett
- Accession number :
- edsair.doi.dedup.....828738684b52db47d894eab91f2ef23f
- Full Text :
- https://doi.org/10.1055/s-2008-1032075