Application of a New Chiral Phosphepine to the Catalytic Asymmetric Synthesis of Highly Functionalized Cyclopentenes That Bear an Array of Heteroatom-Substituted Quaternary Stereocenters
Through the design and synthesis of a new chiral phosphepine, the first catalytic asymmetric method for the [3 + 2] cycloaddition of allenes with olefins has been developed that generates cyclopentenes that bear nitrogen-, phosphorus-, oxygen-, and sulfur-substituted quaternary stereocenters. A wide...
Main Authors: | Fujiwara, Yuji, Fu, Gregory C. |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Chemistry |
Format: | Article |
Language: | en_US |
Published: |
American Chemical Society
2013
|
Online Access: | http://hdl.handle.net/1721.1/82012 |
Similar Items
-
Biphenyl-Derived Phosphepines as Chiral Nucleophilic Catalysts: Enantioselective [4+1] Annulations To Form Functionalized Cyclopentenes
by: Ziegler, Daniel Todd, et al.
Published: (2018) -
Asymmetric nucleophilic substitutions to construct all-carbon quaternary stereocenters under PTC conditions
by: Ban, Xu
Published: (2019) -
Enantioselective carbon–sulfur bond formation: γ additions of aryl thiols to allenoates catalyzed by a chiral phosphepine
by: Fujiwara, Yuji, et al.
Published: (2013) -
Catalytic enantioselective synthesis of oxindoles and benzofuranones bearing a quaternary stereocenter and reactions of palladium bisphosphine complexes relevant to catalytic C-C bond formation
by: Hills, Ivory Derrick, 1977-
Published: (2005) -
Enantioselective synthesis of chiral acyclic nitriles containing α-all-carbon quaternary stereocenters via synergistic palladium and phase-transfer catalysis
by: Guo, Cheng, et al.
Published: (2025)