We are engaged in the systematic efforts to exploit catalytic carbon?carbon (C?C) bond activation for developing new, general and synthetically useful methods. Our objective, in the proposed funding period, is to focus on C?C activation of ketones, as ketone moieties are ubiquitously found in feedstock chemicals, synthetic building blocks and bioactive compounds. Specifically, we will: (i) expand the scope and utilities with activation of strained ketones for constructing complex ring systems, (ii) enable new and broadly applicable transformations with unstrained ketones in an atom-economical fashion, and (iii) explore a new activation mode that can shift the paradigm for ketone activation. The research proposed is expected to simplify synthesis through new strategic bond disconnections, allow for editing skeletons of complex molecules under redox-neutral conditions, and offer a byproduct-free approach to access organic building blocks.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM109054-06S1
Application #
9890419
Study Section
Synthetic and Biological Chemistry B Study Section (SBCB)
Program Officer
Yang, Jiong
Project Start
2013-09-30
Project End
2023-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
6
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Chicago
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Rong, Zi-Qiang; Lim, Hee Nam; Dong, Guangbin (2018) Intramolecular Acetyl Transfer to Olefins by Catalytic C-C Bond Activation of Unstrained Ketones. Angew Chem Int Ed Engl 57:475-479
Xia, Ying; Wang, Jianchun; Dong, Guangbin (2018) Suzuki-Miyaura Coupling of Simple Ketones via Activation of Unstrained Carbon-Carbon Bonds. J Am Chem Soc 140:5347-5351
Zhu, Zixi; Li, Xinghan; Chen, Sicong et al. (2018) Cobalt-Catalyzed Intramolecular Alkyne/Benzocyclobutenone Coupling: C-C Bond Cleavage via a Tetrahedral Dicobalt Intermediate. ACS Catal 8:845-849
Deng, Lin; Jin, Likun; Dong, Guangbin (2018) Fused-Ring Formation by an Intramolecular ""Cut-and-Sew"" Reaction between Cyclobutanones and Alkynes. Angew Chem Int Ed Engl 57:2702-2706
Chen, Peng-Hao; Billett, Brent A; Tsukamoto, Tatsuhiro et al. (2017) ""Cut and Sew"" Transformations via Transition-Metal-Catalyzed Carbon-Carbon Bond Activation. ACS Catal 7:1340-1360
Xia, Ying; Wang, Jianbo; Dong, Guangbin (2017) Distal-Bond-Selective C-C Activation of Ring-Fused Cyclopentanones: An Efficient Access to Spiroindanones. Angew Chem Int Ed Engl 56:2376-2380
Xia, Ying; Lu, Gang; Liu, Peng et al. (2016) Catalytic activation of carbon-carbon bonds in cyclopentanones. Nature 539:546-550
Zhou, Xuan; Dong, Guangbin (2016) Nickel-Catalyzed Chemo- and Enantioselective Coupling between Cyclobutanones and Allenes: Rapid Synthesis of [3.2.2] Bicycles. Angew Chem Int Ed Engl 55:15091-15095
Zhou, Xuan; Ko, Haye Min; Dong, Guangbin (2016) Synthesis of Bridged Cyclopentane Derivatives by Catalytic Decarbonylative Cycloaddition of Cyclobutanones and Olefins. Angew Chem Int Ed Engl 55:13867-13871
Zeng, Rong; Chen, Peng-Hao; Dong, Guangbin (2016) Efficient Benzimidazolidinone Synthesis via Rhodium-Catalyzed Double-Decarbonylative C-C Activation/Cycloaddition between Isatins and Isocyanates. ACS Catal 6:969-973

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