Synthetic Studies on the Taxane Skeleton: Construction of Eight-Membered Carbocyclic Rings by the Intramolecular B-Alkyl Suzuki−Miyaura Cross-Coupling Reaction
Organic Letters2004Vol. 6(24), pp. 4491–4494
Citations Over TimeTop 20% of 2004 papers
Abstract
Construction of eight-membered carbocyclic rings via the intramolecular B-alkyl Suzuki-Miyaura cross-coupling reaction has been studied. This protocol proved its potency through the formation of the eight-membered ring possessing a quaternary carbon on its ring in high yield, affording promise of a new access to the eight-membered ring of Taxol. [reaction: see text]
Related Papers
- → Intramolecular Hydrogen Bond Interaction in Selected Diols(2003)17 cited
- → Intramolecular isotope effects in the reactions of CF32+ and CO22+ with HD(2001)28 cited
- → Nature of weak inter-and intramolecular interactions in crystals 8. Influence of intermolecular contacts on the strength of intramolecular O-H...N bonds in crystals of 3-(2-hydroxyphenyl)-1,2,4-triazoles(2006)3 cited
- → Stimulation intramolecular F⋯H hydrogen bond by intramolecular N → Si interaction in Si-fluoro derivatives of 8-mercaptoquinoline: DFT and MP2 calculations(2018)1 cited
- Conformations and Intramolecular Hydrogen Bonds of a Series of Amino-alcohols(2013)