grant

Metal-Catalyzed Methods for Organic Synthesis

Organization MASSACHUSETTS INSTITUTE OF TECHNOLOGYLocation CAMBRIDGE, UNITED STATESPosted 1 Jun 2017Deadline 31 May 2027
NIHUS FederalResearch GrantFY2025AcademiaAgricultural ChemicalsAgrochemicalsAlkenesAminesAreaBenignBiomedical ResearchCarbonChemistryComplexCopperCouplingCu elementDevelopmentDrug IndustryEnvironmentF elementFluorineGroup ProcessesHealthHumanImprove AccessIndustryLeadLigandsMetalsMethodsModern ManMolecularNatural ProductsNitrogenO elementO2 elementOlefinsOrganic ChemistryOrganic SynthesisOxygenPalladiumPb elementPd elementPharmaceutic IndustryPharmaceutical AgentPharmaceutical IndustryPharmaceuticalsPharmacologic SubstancePharmacological SubstancePreparationProcessPropertySensoryTechniquesWorkamineanalogcatalystdesigndesigningdevelopmentaldrug developmentdrug discoveryheavy metal Pbheavy metal leadimprovedinventionnaturally occurring productnew technologynovel technologiespharmaceuticalpreparationsscale upside effectsocial group processuser-friendly
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Full Description

Project Summary/Abstract:
The ability to systematically construct highly functionalized molecules in a general and reliable manner

is central to synthetic organic chemistry and key for drug discovery, development, and scale-up in both

academia and, in particular, the pharmaceutical industry. Our proposed work includes palladium-

catalyzed cross coupling methods for the formation of aromatic and heterocyclic carbon-nitrogen bonds,

carbon-oxygen bonds and carbon-fluorine bonds. One aspect of the chemistry that we are proposing

involves the design of improved ligands and methods for aromatic carbon-heteroatom bond formation.

Our work in this area is used throughout academia and industry for the preparation of complex molecules

and has become mainstay processes for synthetic chemists. As part of this, we have developed

numerous new ligands and catalysts that are now commercially available and widely employed. The

invention of new, more general, and more user-friendly techniques will not only allow access to important

compounds but also the means to be able to efficiently and selectively modify them. This allows chemists

to rationally make new derivatives, with decreased side effects and better properties. We are also working

on copper-catalyzed methods for the highly regio-, diastereo-, and enantioselective synthesis of aliphatic

amines, copper-catalyzed methods for the asymmetric formation of carbon-carbon bonds and dual

copper- and palladium-catalyzed processes. A portion of this work aims to design new more

economically, environmentally, and generally applicable methods for the formation of carbon-carbon

bonds by using alkenes as pronucleophiles. We wish to develop chemistry that will allow us to replace

standard, highly reactive reactants with more benign and useful ones. We will also carry out mechanistic

studies to help understand the fundamental features of these transformations and to help guide us in

advancing the efficiency and utility of this work. The substrates we are targeting are representative of

common structural components found in pharmaceuticals, natural products, agrochemicals, and sensory

materials. The availability of these new technologies will allow others to prepare a variety of highly-

functionalized and structurally diverse compounds, many of which have previously been inaccessible,

which will have a great impact in a range of areas that are directly important to human health.

Grant Number: 5R35GM122483-09
NIH Institute/Center: NIH

Principal Investigator: STEPHEN BUCHWALD

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