E-mail a Wiley Online Library Link

Prof. Dr. Li-Wen Xu Powerful Amino Acid Derived Bifunctional Phosphine Catalysts Bearing a Hydrogen Bond Donor in Asymmetric Synthesis ChemCatChem 5

Version of Record online: 21 MAY 2013 | DOI: 10.1002/cctc.201300198

Thumbnail image of graphical abstract

Phosphines and hydrogen bonding are good collaborators! Air-stable α-amino acids or dipeptide derived chiral phosphines bearing hydrogen-bond-donating and silicon-based bulky groups are powerful and versatile catalysts for a range of enantioselective processes, including [3+2] and [4+2] cycloadditions, allylic alkylations, Morita–Baylis–Hillman reactions, and Michael addition reactions. They represent a class of novel, economical, and practical chiral phosphine-based organocatalysts.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field