2452697
Project Grant
Overview
Grant Description
Cross-nucleophile coupling and homologation reactions of organoboron compounds - with support from the Chemical Synthesis Program in the Division of Chemistry, Professor Gojko Lalic at the University of Washington is studying the development of new reactions for the synthesis of organic molecules using organoboron compounds and transition metal catalysis.
The project is advancing more efficient transformations of common starting materials into more valuable targets, complementing existing methods.
These reactions are providing a new approach to forming carbon-carbon bonds, critical for constructing large organic molecules.
Beyond practical applications in organic synthesis, the fundamental properties and reactivity of organoboron compounds are being investigated and expanded in these studies.
An essential part of the project is its outreach initiative, which fosters connections with the local community.
Dr. Lalic's team engages elementary and high school students through activities that inspire interest in science, technology, engineering, and mathematics (STEM) careers.
Organoboron compounds are valuable synthetic building blocks due to their availability, stability, and versatile reactivity.
Continued advances in the synthetic applications of these compounds is critically important to support the pharmaceutical industry, medicinal chemistry, the synthesis of agrochemicals, and material science.
Prof. Lalic and his research team are creating more effective tools for synthesizing complex organic molecules by exploring two new classes of chemical reactions.
The first is a new type of cross-coupling reaction using two nucleophilic coupling partners that leverages the ambiphilic nature of organoboron compounds and the ability of transition metal complexes to modulate their reactivity.
The second focuses on innovative strategies for homologating organoboron compounds via formal insertion of C2 fragments into carbon-boron bonds.
Notably, this C2 fragment insertion involves an unusually facile activation of carbon-carbon bonds.
Integral to this work are outreach activities, which are designed in collaboration with the local community, to promote science education and engagement.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the foundation's intellectual merit and broader impacts review criteria.
Subawards are not planned for this award.
The project is advancing more efficient transformations of common starting materials into more valuable targets, complementing existing methods.
These reactions are providing a new approach to forming carbon-carbon bonds, critical for constructing large organic molecules.
Beyond practical applications in organic synthesis, the fundamental properties and reactivity of organoboron compounds are being investigated and expanded in these studies.
An essential part of the project is its outreach initiative, which fosters connections with the local community.
Dr. Lalic's team engages elementary and high school students through activities that inspire interest in science, technology, engineering, and mathematics (STEM) careers.
Organoboron compounds are valuable synthetic building blocks due to their availability, stability, and versatile reactivity.
Continued advances in the synthetic applications of these compounds is critically important to support the pharmaceutical industry, medicinal chemistry, the synthesis of agrochemicals, and material science.
Prof. Lalic and his research team are creating more effective tools for synthesizing complex organic molecules by exploring two new classes of chemical reactions.
The first is a new type of cross-coupling reaction using two nucleophilic coupling partners that leverages the ambiphilic nature of organoboron compounds and the ability of transition metal complexes to modulate their reactivity.
The second focuses on innovative strategies for homologating organoboron compounds via formal insertion of C2 fragments into carbon-boron bonds.
Notably, this C2 fragment insertion involves an unusually facile activation of carbon-carbon bonds.
Integral to this work are outreach activities, which are designed in collaboration with the local community, to promote science education and engagement.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the foundation's intellectual merit and broader impacts review criteria.
Subawards are not planned for this award.
Awardee
Funding Goals
THE GOAL OF THIS FUNDING OPPORTUNITY, "DIVISION OF CHEMISTRY: DISCIPLINARY RESEARCH PROGRAMS", IS IDENTIFIED IN THE LINK: HTTPS://WWW.NSF.GOV/PUBLICATIONS/PUB_SUMM.JSP?ODS_KEY=NSF22605
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Seattle,
Washington
98195-1016
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 100% from $300,000 to $600,000.
University Of Washington was awarded
Project Grant 2452697
worth $600,000
from the Division of Chemistry in July 2025 with work to be completed primarily in Seattle Washington United States.
The grant
has a duration of 3 years and
was awarded through assistance program 47.049 Mathematical and Physical Sciences.
The Project Grant was awarded through grant opportunity Division of Chemistry: Disciplinary Research Programs.
Status
(Ongoing)
Last Modified 9/10/25
Period of Performance
7/1/25
Start Date
6/30/28
End Date
Funding Split
$600.0K
Federal Obligation
$0.0
Non-Federal Obligation
$600.0K
Total Obligated
Activity Timeline
Transaction History
Modifications to 2452697
Additional Detail
Award ID FAIN
2452697
SAI Number
None
Award ID URI
SAI EXEMPT
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
490309 DIVISION OF CHEMISTRY
Funding Office
490309 DIVISION OF CHEMISTRY
Awardee UEI
HD1WMN6945W6
Awardee CAGE
1HEX5
Performance District
WA-07
Senators
Maria Cantwell
Patty Murray
Patty Murray
Modified: 9/10/25