Supporting Information
| Supporting Information File 1: Detailed experimental procedures, copies of 1H and 13C NMR spectra for the new compounds and chiral HPLC reports. | ||
| Format: PDF | Size: 1.4 MB | Download |
Cite the Following Article
Total synthesis of (+)-grandiamide D, dasyclamide and gigantamide A from a Baylis–Hillman adduct: A unified biomimetic approach
Andivelu Ilangovan and Shanmugasundar Saravanakumar
Beilstein J. Org. Chem. 2014, 10, 127–133.
https://doi.org/10.3762/bjoc.10.9
How to Cite
Ilangovan, A.; Saravanakumar, S. Beilstein J. Org. Chem. 2014, 10, 127–133. doi:10.3762/bjoc.10.9
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Scholarly Works
- Takagi, R.; Fujii, E.; Kondo, H. Enantioselective Michael Reaction of Cyclic β-Ketoesters with Morita–Baylis–Hillman Derivatives Using a Phase-Transfer Catalyst. The Journal of organic chemistry 2018, 83, 11191–11203. doi:10.1021/acs.joc.8b01777
- Basavaiah, D.; Naganaboina, R. T. The Baylis–Hillman reaction: a new continent in organic chemistry – our philosophy, vision and over three decades of research. New Journal of Chemistry 2018, 42, 14036–14066. doi:10.1039/c8nj02483a
- Bharadwaj, K. C. Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions. A catalytic and atom economic route for carbocycles and heterocycles. RSC Advances 2015, 5, 75923–75946. doi:10.1039/c5ra13611c
