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Enantioselective desymmetrizing hydroamination to synthesize complex all-carbon quaternary stereocenter containing saturated heterocyclic structures

Award Number: R15GM160943
ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 09/01/2025
PERIOD OF PERFORMANCE END DATE: 08/31/2028

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Enantioselective desymmetrizing hydroamination to synthesize complex all-carbon quaternary stereocenter containing saturated heterocyclic structures - Project Summary/Abstract Heterocyclic rings and tetrahedral carbons are common components of successful small molecule drugs. The polarity and hydrogen bonding capability of heterocyclic rings promotes solubility in aqueous solutions and provides opportunities for critical intermolecular force interactions with protein targets, thereby promoting drug-protein binding affinity. Tetrahedral carbons in drugs create selective interactions with protein targets thereby minimizing unwanted side effects due to interactions with non-target proteins or other biomolecules. Tetrahedral carbons are also believed to facilitate small molecule dissolution because more three-dimensional molecules pack less efficiently into the solid phase and therefore more readily separate. All-carbon quaternary carbons are one of the most difficult types of tetrahedral carbons and are common in bioactive molecules, especially those found in nature. In fact, structure searches of fused heterocyclic rings with quaternary carbons at the bridgehead are found by the thousands in bioactive molecules, yet there is no general synthetic tool to enantioselectively construct these molecules. The current proposal describes an efficient synthetic tool to enantioselectively construct fused heterocyclic compounds with bridgehead quaternary carbons from inexpensive benzoic acid derivatives in four or five steps. The method generates symmetrical cyclohexadiene structures from Birch reduction-alkylation reactions of benzoic acid derivatives and then desymmetrizes them through enantioselective alkene hydroamination reactions. The proposal will explore the use of chiral copper catalysts to facilitate the enantioselective desymmetrizing hydroamination reaction. Copper has the advantage of both low cost and being environmentally benign. The research would build on the enantioselective desymmetrizing Mizoroki- Heck reactions that we have previously reported for both palladium and nickel chiral catalysts. It also seeks to extend the impressive copper-catalyzed hydroamination work by other researchers to enantioselective desymmetrizing reactions. Critical to the reaction development will be the use of computational chemistry to model the key amino- cupration step, which is the likely rate and enantioselectivity determining step based on literature precedent. Leveraging our experience with understanding the basis of enantioselectivity in the analogous 1,2-insertion of the desymmetrizing Ni-catalyzed Mizoroki-Heck reaction, we will accelerate the search for optimal chiral ligands by modeling the key amino-cupration step. Most importantly, the project will provide three undergraduate students and one graduate student with exposure to and training in contemporary synthetic chemistry reaction development to address an important deficiency in the armamentarium of synthetic tools for complex molecule synthesis in the 21st century.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2025 ( Subtotal = $548,701 )
2025	2025	BRYN MAWR COLLEGE	101 N MERION AVE	BRYN MAWR	PA	19010	DELAWARE	USA	Biomedical Research and Research Training	000	1	8/25/2025	NEW	$548,701
														Subtotal = $548,701

Grand Total All Awards = $548,701

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Enantioselective desymmetrizing hydroamination to synthesize complex all-carbon quaternary stereocenter containing saturated heterocyclic structures

Award Number: R15GM160943

ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 09/01/2025

PERIOD OF PERFORMANCE END DATE: 08/31/2028

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