摘要
The first asymmetric Michael addition of α-aryl cyclopentanones to nitroolefins for construction of adjacent quaternary and tertiary stereocenters has been achieved with excellent diastereo-/enantioselectivity.
源语言 | 英语 |
---|---|
页(从-至) | 6840-6842 |
页数 | 3 |
期刊 | Chemical Communications |
卷 | 46 |
期 | 36 |
DOI | |
出版状态 | 已出版 - 28 9月 2010 |
已对外发布 | 是 |
指纹
探究 'Organocatalytic asymmetric Michael addition of α-aryl cyclopentanones to nitroolefins for construction of adjacent quaternary and tertiary stereocenters' 的科研主题。它们共同构成独一无二的指纹。引用此
Dong, X. Q., Teng, H. L., Tong, M. C., Huang, H., Tao, H. Y., & Wang, C. J. (2010). Organocatalytic asymmetric Michael addition of α-aryl cyclopentanones to nitroolefins for construction of adjacent quaternary and tertiary stereocenters. Chemical Communications, 46(36), 6840-6842. https://doi.org/10.1039/c0cc01987a