Supporting Information
| Supporting Information File 1: Experimental methods including detailed synthetic procedures, compound characterization data, and DFT calculations. | ||
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| Supporting Information File 2: Crystallographic information file of compound 3a. | ||
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| Supporting Information File 3: Crystallographic information file of compound 6b. | ||
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Cite the Following Article
Regioselectively α- and β-alkynylated BODIPY dyes via gold(I)-catalyzed direct C–H functionalization and their photophysical properties
Takahide Shimada, Shigeki Mori, Masatoshi Ishida and Hiroyuki Furuta
Beilstein J. Org. Chem. 2020, 16, 587–595.
https://doi.org/10.3762/bjoc.16.53
How to Cite
Shimada, T.; Mori, S.; Ishida, M.; Furuta, H. Beilstein J. Org. Chem. 2020, 16, 587–595. doi:10.3762/bjoc.16.53
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Scholarly Works
- Nguyen, Y. T.; Shin, S.; Kwon, K.; Kim, N.; Bae, S. W. BODIPY-based fluorescent sensors for detection of explosives. Journal of Chemical Research 2023, 47, 174751982311689. doi:10.1177/17475198231168961
- Prabagar, B.; Shi, Z. doi:10.1002/9781119774167.ch2
- Le Du, E.; Waser, J. Recent progress in alkynylation with hypervalent iodine reagents. Chemical communications (Cambridge, England) 2023, 59, 1589–1604. doi:10.1039/d2cc06168f
- Gupta, A.; Chakraborty, S.; Ghosh, D.; Ramakrishnan, R. Data-driven modeling of S0 → S1 excitation energy in the BODIPY chemical space: High-throughput computation, quantum machine learning, and inverse design. The Journal of chemical physics 2021, 155, 244102. doi:10.1063/5.0076787
- Dzyuba, S. V. BODIPY Dyes as Probes and Sensors to Study Amyloid-β-Related Processes. Biosensors 2020, 10, 192. doi:10.3390/bios10120192
