X. Gu
A general, scalable, organocatalytic nitro-Michael addition to enones: Enantioselective access to all-carbon quaternary stereocenters
Gu, X.; Dai, Y.; Guo, T.; Franchino, A.; Dixon∗, D.J.; Ye∗, J.
Authors
Y. Dai
T. Guo
Dr Allegra Franchino allegra.franchino@durham.ac.uk
Assistant Professor
D.J. Dixon∗
J. Ye∗
Citation
Gu, X., Dai, Y., Guo, T., Franchino, A., Dixon∗, D., & Ye∗, J. (2015). A general, scalable, organocatalytic nitro-Michael addition to enones: Enantioselective access to all-carbon quaternary stereocenters. Organic Letters, 17, https://doi.org/10.1021/acs.orglett.5b00387
| Journal Article Type | Article |
|---|---|
| Online Publication Date | Mar 11, 2015 |
| Publication Date | 2015 |
| Deposit Date | Feb 20, 2023 |
| Journal | Organic Letters |
| Print ISSN | 1523-7060 |
| Electronic ISSN | 1523-7052 |
| Publisher | American Chemical Society |
| Volume | 17 |
| DOI | https://doi.org/10.1021/acs.orglett.5b00387 |
| Public URL | https://durham-repository.worktribe.com/output/1181507 |
You might also like
Late-stage diversification of indole skeletons through nitrogen atom insertion
(2022)
Journal Article
H-Bonded counterion-directed enantioselective Au(I) catalysis
(2022)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search