Natural Product Synthesis as an Inspiration for Method Development and Biological Studies

Date:2019-05-16Clicks:21设置

Topic: Natural Product Synthesis as an Inspiration for Method Development and Biological Studies

Speaker: Professor Paul E. Floreancig

Event date: 5/16/2019

Event time: 16:10 p.m.

Venue: Room 211, Building 20

Sponsor: School of Chemistry & Materials Science, Institute of Science and Technology

Publications of the Speaker:

1) Caplan, S. M.; Floreancig, P. E. Total Synthesis of Divergolides E and H Angew. Chem., Int. Ed. 2018, 57, 15866-15870. DOI: 10.1002/anie.201810336.

2) Qin, Q.; Xie, Y.; Floreancig, P. E. Diarylmethane Synthesis through Re2O7-Catalyzed Bimolecular Dehydrative Friedel–Crafts Reactions Chem. Sci. 2018, 9, 8528-8534. DOI: 10.1039/C8SC03570A.

3) Morales-Rivera, C. A.; Floreancig, P. E.; Liu, P. Predictive Model for Oxidative C–H Functionalization Reactivity with 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone J. Am. Chem. Soc. 2017, 139, 17935-17944. DOI: 10.1021/jacs.7b08902.

4) Rohrs, T. M.; Qin, Q.; Floreancig, P. E. Re2O7-Mediated Dehydrative Cyclization Reactions: Application to the Total Synthesis of Herboxidiene and an Analog Angew. Chem., Int. Ed. 2017, 56, 10900-10904. DOI: 10.1002/anie.201705924.

5) Hanna, R. D.; Naro, Y.; Deiters, A.; Floreancig, P. E. Alcohol, Aldehyde, and Ketone Liberation and Intracellular Cargo Release through Peroxide-Mediated Boryl Ether Fragmentation J. Am. Chem. Soc. 2016, 138, 13353-13360. DOI: 10.1021/jacs.6b07890.

6) Han, X.; Floreancig, P. E. Spiroacetal Formation through Telescoped Cycloaddition and Carbon–Hydrogen Bond Functionalization: Total Synthesis of Bistramide A Angew. Chem., Int. Ed. 2014, 53, 11075-11078. DOI: 10.1002/anie.201406819.

7) Xie, Y.; Floreancig, P. E. Allylic Alcohol Transposition-Based Heterocycle Synthesis Using Traceless Trapping Groups Angew. Chem., Int. Ed. 2014, 53, 4926-4929. DOI: 10.1002/anie201402010.

8) Xie, Y.; Floreancig, P. E. Cascade Approach to Stereoselective Polycyclic Ether Formation: Epoxides as Trapping Agents in the Transposition of Allylic Alcohols Angew. Chem., Int. Ed. 2013, 52, 625-628. DOI: 10.1002/anie.201208132.


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