New organic reactions that employ Lewis bases (nucleophiles) as catalysts have received much less attention than the corresponding areas of Lewis acid catalysis or transition metal catalysis. However, this Lewis base strategy can access innovative and different reactivity patterns unattainable with these established catalysis approaches. The long range goals of these studies are to develop new polarity reversal reactions (Umpolung) catalyzed by Lewis bases and to uncover the fundamental interactions/characteristics that guide them. Our approach focuses on fully developing our recently discovered nucleophile-catalyzed carbonyl anion addition reaction employing acylsilanes and a-keto acids. These processes rely on the insight that acylsilanes and a-keto acids are viable carbonyl anion precursors when exposed to the correct catalytic additions. The use of acylsilanes and a-keto acids as practical acyl anion precursors avoids the potential problem of benzoin formation incurred when using aldehydes as acyl anion precursors. Furthermore, the anions generated from these precursors using achiral and chiral Lewis bases will be added to prochiral electrophiles to produce high value compounds that are immensely important in the construction of health- improving materials such as Pharmaceuticals and compounds to be used as biological probes. Additional related focuses of this proposal include the discovery and development of two related Umpolung reactions: catalytic homoenolate additions and stereoselective vinylogous carbonyl anion additions. These novel, unconventional bond-forming strategies have significant potential to efficiently access target-oriented or diversity-oriented molecules of interest. The proposed research explores the general applicability our organocatalytic carbonyl anion strategies for rapidly synthesizing molecules that directly impact human health. Each of these processes has mechanistic aspects to explore that will provide general information regarding nucleophile-catalyzed processes. In addition, a strong emphasis has been placed on the development of new Lewis base catalysts (achiral and chiral) in order to render many of our current reactions stereoselective. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM073072-03
Application #
7488762
Study Section
Synthetic and Biological Chemistry B Study Section (SBCB)
Program Officer
Schwab, John M
Project Start
2006-09-20
Project End
2011-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
3
Fiscal Year
2008
Total Cost
$238,396
Indirect Cost
Name
Northwestern University at Chicago
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Hovey, M Todd; Cohen, Daniel T; Walden, Daniel M et al. (2017) A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Angew Chem Int Ed Engl 56:9864-9867
Murauski, Kathleen J R; Walden, Daniel M; Cheong, Paul Ha-Yeon et al. (2017) A Cooperative Ternary Catalysis System for Asymmetric Lactonizations of ?-Ketoesters. Adv Synth Catal 359:3713-3719
Sharma, Hayden A; Todd Hovey, M; Scheidt, Karl A (2016) Azaindole synthesis through dual activation catalysis with N-heterocyclic carbenes. Chem Commun (Camb) 52:9283-6
Wang, Michael H; Cohen, Daniel T; Schwamb, C Benjamin et al. (2015) Enantioselective ?-Protonation by a Cooperative Catalysis Strategy. J Am Chem Soc 137:5891-4
Lee, Anna; Scheidt, Karl A (2015) N-Heterocyclic carbene-catalyzed enantioselective annulations: a dual activation strategy for a formal [4+2] addition for dihydrocoumarins. Chem Commun (Camb) 51:3407-10
Cohen, Daniel T; Johnston, Ryne C; Rosson, Nicholas T et al. (2015) Functionalized cyclopentenes through a tandem NHC-catalyzed dynamic kinetic resolution and ambient temperature decarboxylation: mechanistic insight and synthetic application. Chem Commun (Camb) 51:2690-3
Liu, Kun; Hovey, M Todd; Scheidt, Karl A (2014) A Cooperative N-Heterocyclic Carbene/Palladium Catalysis System. Chem Sci 5:4026-4031
Lee, Anna; Younai, Ashkaan; Price, Christopher K et al. (2014) Enantioselective annulations for dihydroquinolones by in situ generation of azolium enolates. J Am Chem Soc 136:10589-92
Lee, Anna; Scheidt, Karl A (2014) A cooperative N-heterocyclic carbene/chiral phosphate catalysis system for allenolate annulations. Angew Chem Int Ed Engl 53:7594-8
Hovey, M Todd; Check, Christopher T; Sipher, Alexandra F et al. (2014) N-heterocyclic-carbene-catalyzed synthesis of 2-aryl indoles. Angew Chem Int Ed Engl 53:9603-7

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