This program has as its objectives the discovery, development, and application of selective catalytic reactions of use in organic synthesis. In particular, the focus of our research is on catalytic reactions that generate optically active products from achiral or racemic starting materials. We seek to identify catalysts for asymmetric reactions of broad synthetic utility, to elucidate the reaction mechanisms of these reactions, and to illustrate their utility through their application in the efficient synthesis of useful building blocks and complex targets. We have developed highly effective transition metal, main group metal, and organic catalyst systems for asymmetric synthesis. Cooperative reactivity between catalyst reactive sites has been identified asa powerful strategy for stereochemical control of nucleophile-electrophile reactions. Many of the reactions we plan to investigate rely on the design of catalyst systems that effect dual activation of reacting partners within a chiral framework.
Our aim i s to discover chiral frameworks,which we have coined """"""""privileged chiral ligands"""""""", that display high enantioselectivity across a broad range of mechanisms. In addition, we seek catalyst systems that display extraordinary generality across a range of substrate combinations. Our efforts to this point have revealed that such breadth of scope is not only possible, but quite common. Through careful screening and design of new catalystsand investigation of their reaction mechanisms, we seek to elucidate the basis of these surprising generality phenomena in asymmetric catalysis. Ultimately, we anticipate that these studies will not only lead to catalystsfor valuable organic reactions, but also lay the principles that will allow rational design of new, broadly effective catalysts. During the coming grant period, our efforts will be directed toward the discovery of enantioselective additions of carbon-centerednucleophiles to epoxides, imines, alkylhalides, and a,(3-unsaturated carbonyl systems. The generation of chiral (handed) compounds efficiently and in pure form stands as one of the most important challenges in synthetic chemistry, partly due to the difficulty of the challenge, and partly due to the prevalence of chirality in Nature. This program aims to impact public health through the development of catalysts that will find widespread application for the practicalsynthesis of pharmaceuticals and other biologically important compounds.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
4R37GM043214-17
Application #
7318384
Study Section
Special Emphasis Panel (NSS)
Program Officer
Schwab, John M
Project Start
1991-01-01
Project End
2011-12-31
Budget Start
2007-03-01
Budget End
2007-12-31
Support Year
17
Fiscal Year
2007
Total Cost
$497,147
Indirect Cost
Name
Harvard University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Wendlandt, Alison E; Vangal, Prithvi; Jacobsen, Eric N (2018) Quaternary stereocentres via an enantioconvergent catalytic SN1 reaction. Nature 556:447-451
Zhou, Biying; Haj, Moriana K; Jacobsen, Eric N et al. (2018) Mechanism and Origins of Chemo- and Stereoselectivities of Aryl Iodide-Catalyzed Asymmetric Difluorinations of ?-Substituted Styrenes. J Am Chem Soc 140:15206-15218
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Banik, Steven M; Mennie, Katrina M; Jacobsen, Eric N (2017) Catalytic 1,3-Difunctionalization via Oxidative C-C Bond Activation. J Am Chem Soc 139:9152-9155
Park, Yongho; Harper, Kaid C; Kuhl, Nadine et al. (2017) Macrocyclic bis-thioureas catalyze stereospecific glycosylation reactions. Science 355:162-166
Turek, Amanda K; Hardee, David J; Ullman, Andrew M et al. (2016) Activation of Electron-Deficient Quinones through Hydrogen-Bond-Donor-Coupled Electron Transfer. Angew Chem Int Ed Engl 55:539-44
Lehnherr, Dan; Ford, David D; Bendelsmith, Andrew J et al. (2016) Conformational Control of Chiral Amido-Thiourea Catalysts Enables Improved Activity and Enantioselectivity. Org Lett 18:3214-7

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