Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1324584 | Journal of Organometallic Chemistry | 2009 | 10 Pages |
Fruitful methods for the preparation of various (poly)unsaturated, (poly)cyclic and cage organic compounds with the use of allylic type organoboranes have been developed. Allylborane reactions proceeding with the rearrangement of allylic moiety or via a direct rupture of the B–C bond (with retention) little known to the boron community are considered. Synthesis of boron containing clathrochelates and some transformations of 1-boraadamantane, a unique cage compound, are also described.
Graphical abstractAllylboranes reactions proceeding with the rearrangement of allylic moiety or via a direct rupture of the B–C bond (with retention) have been used for the preparation of various unsaturated, cyclic and cage compounds.Figure optionsDownload full-size imageDownload as PowerPoint slide