| Title: | Highly diastereoselective synthesis of substituted cyclopentenes through multicomponent reactions of phosphines, enynedioates, and benzylidene malononitriles via an unexpected phosphine alpha-addition-delta-evolvement of an anion pathway |
| Authors: | Chuang, Shih-Ching Sung, Shih-Ping 應用化學系 Department of Applied Chemistry |
| Issue Date: | 13-Mar-2016 |
| URI: | http://hdl.handle.net/11536/144970 |
| ISSN: | 0065-7727 |
| Journal: | ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY |
| Volume: | 251 |
| Appears in Collections: | Articles |
- Multicomponent reactions of phosphines, enynedioates and benzylidene malononitriles generated highly substituted cyclopentenes through an unexpected phosphine alpha-addition-delta-evolvement of an anion pathway / Chuang, Shih-Ching;Sung, Shih-Ping;Deng, Jie-Cheng;Chiou, Mong-Feng;Hsu, Day-Shin
- Multicomponent Reactions of Phosphines, Diynedioates, and Aryl Aldehydes Generated Furans Appending Reactive Phosphorus Ylides through Cumulated Trienoates as Key Intermediates: A Phosphine alpha-Addition-delta-Evolvement of an Anion Pathway / Deng, Jie-Cheng;Chuang, Shih-Ching
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