Substrate-controlled, phosphine-catalyzed domino reactions of activated conjugated dienes: highly diastereoselective synthesis of bicyclic skeletons.

Abstract

The introduction of the domino reaction as a concept in organic synthesis has inspired fruitful discoveries. A successful domino reaction depends on the selection of efficient catalysts and appropriate substrates. Our group is focused on the study of phosphine-catalyzed domino reactions based on the Morita– Baylis–Hillman (MBH) reaction and the Rauhut… (More)
DOI: 10.1002/chem.201100881

Topics

3 Figures and Tables

Cite this paper

@article{Ma2011SubstratecontrolledPD, title={Substrate-controlled, phosphine-catalyzed domino reactions of activated conjugated dienes: highly diastereoselective synthesis of bicyclic skeletons.}, author={Jianze Ma and Peizhong Xie and Chongchong Hu and You Huang and Ruyu Chen}, journal={Chemistry}, year={2011}, volume={17 27}, pages={7418-22} }