← Leaderboards
Gregory C Fu
Massachusetts Institute Of Technology
$25,072,567
Attributed
$25,072,567
Total exposure
6
Grants
6
Lead (contact PI)
Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants. They are the sole PI on all grants (the two match).
Funding over time
peak $1.6M · FY2005–25$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$25,072,567 · 6
By mechanism
R01$16,010,162 · 4
R37$5,486,498 · 1
R35$3,575,907 · 1
Top collaborators
No co-investigators on record.
Most similar at Massachusetts Institute Of Technology
Same institution · by research overlap
- Timothy F Jamison$5,905,508
- Alexander T Radosevich$4,284,121
- Ronald T Raines$23,937,707
- Rick L Danheiser$2,850,597
- Richard R Schrock$9,534,153
Others in their field
Top investigators on “Catalyst”
- Lee Marshall Nadler · Dana-Farber Cancer Inst$152,553,147
- Steven E Reis · University Of Pittsburgh At Pittsburgh$110,730,780
- Rebecca Montalvan · Westat, Inc.$86,600,000
- Mary L. Disis · University Of Washington$47,475,880
- Steven M. Dubinett · Va Greater Los Angeles Healthcare System$43,684,197
- Huw M Davies · Suny At Buffalo$43,386,311
Research focus
CatalystReactionOrganic SynthesisBiochemistryPharmaceutical ChemistryDisciplineBiologyInvestigationHandednessFamilyCouplingTransition ElementsBiologicalProgramsMetalsCarbonBasePlayCommunitiesGrantLifeEnantiomerNickelGenerations
Grant awards (67)
Metal-Catalyzed Nucleophilic Substitution Reactions of Alkyl Electrophiles$967,370
R35 · FY2025 · GM · contact PI
Metal-Catalyzed Nucleophilic Substitution Reactions of Alkyl Electrophiles$967,370
R35 · FY2024 · GM · contact PI
Metal-Catalyzed Nucleophilic Substitution Reactions of Alkyl Electrophiles$967,370
R35 · FY2023 · GM · contact PI
Metal-Catalyzed Nucleophilic Substitution Reactions of Alkyl Electrophiles$12,920
R35 · FY2023 · GM · contact PI
Metal-Catalyzed Nucleophilic Substitution Reactions of Alkyl Electrophiles$660,877
R35 · FY2022 · GM · contact PI
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles$626,905
R01 · FY2022 · GM · contact PI
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles$626,905
R01 · FY2021 · GM · contact PI
PHOTOINDUCED, COPPER-CATALYZED SUBSTITUTION REACTIONS OF ALKYL ELECTROPHILES BY NITROGEN NUCLEOPHILES$432,313
R01 · FY2021 · GM · contact PI
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles$122,045
R01 · FY2021 · GM · contact PI
Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles$626,905
R01 · FY2020 · GM · contact PI
PHOTOINDUCED, COPPER-CATALYZED SUBSTITUTION REACTIONS OF ALKYL ELECTROPHILES BY NITROGEN NUCLEOPHILES$487,840
R01 · FY2020 · GM · contact PI
Helium Recovery System$246,760
R01 · FY2020 · GM · contact PI
Photoinduced, Copper-Catalyzed Substitution Reactions of Alkyl Electrophiles by Nitrogen Nucleophiles$224,213
R01 · FY2020 · GM · contact PI
PHOTOINDUCED, COPPER-CATALYZED SUBSTITUTION REACTIONS OF ALKYL ELECTROPHILES BY NITROGEN NUCLEOPHILES$543,365
R01 · FY2019 · GM · contact PI
Metal-Catalyzed Coupling Reactions$537,105
R37 · FY2019 · GM · contact PI
PHOTOINDUCED, COPPER-CATALYZED SUBSTITUTION REACTIONS OF ALKYL ELECTROPHILES BY NITROGEN NUCLEOPHILES$55,527
R01 · FY2019 · GM · contact PI
Metal-Catalyzed Coupling Reactions$537,105
R37 · FY2018 · GM · contact PI
PHOTOINDUCED, COPPER-CATALYZED SUBSTITUTION REACTIONS OF ALKYL ELECTROPHILES BY NITROGEN NUCLEOPHILES$432,313
R01 · FY2018 · GM · contact PI
Metal-Catalyzed Coupling Reactions$169,375
R37 · FY2018 · GM · contact PI
Metal-Catalyzed Coupling Reactions$537,105
R37 · FY2017 · GM · contact PI
Photoinduced, Copper-Catalyzed C-N Coupling Reactions$355,093
R01 · FY2017 · GM · contact PI
Metal-Catalyzed Coupling Reactions$537,105
R37 · FY2016 · GM · contact PI
Photoinduced, Copper-Catalyzed C-N Coupling Reactions$355,093
R01 · FY2016 · GM · contact PI
Metal-Catalyzed Coupling Reactions$571,080
R37 · FY2015 · GM · contact PI
Photoinduced, Copper-Catalyzed C-N Coupling Reactions$431,090
R01 · FY2015 · GM · contact PI
Metal-Catalyzed Coupling Reactions$510,793
R37 · FY2014 · GM · contact PI
Photoinduced, Copper-Catalyzed C-N Coupling Reactions$335,342
R01 · FY2014 · GM · contact PI
Photoinduced, Copper-Catalyzed C-N Coupling Reactions$50,337
R01 · FY2014 · GM · contact PI
Metal-Catalyzed Coupling Reactions$492,915
R37 · FY2013 · GM · contact PI
Asymmetric Nucleophilic Catalysis$366,111
R01 · FY2013 · GM · contact PI
Metal-Catalyzed Coupling Reactions$383,397
R37 · FY2012 · GM · contact PI
Asymmetric Nucleophilic Catalysis$250,644
R01 · FY2012 · GM · contact PI
Asymmetric Nucleophilic Catalysis$127,238
R01 · FY2012 · GM · contact PI
Metal-Catalyzed Coupling Reactions$118,727
R37 · FY2012 · GM · contact PI
Metal-Catalyzed Coupling Reactions$515,656
R37 · FY2011 · GM · contact PI
Asymmetric Nucleophilic Catalysis$388,652
R01 · FY2011 · GM · contact PI
Metal-Catalyzed Coupling Reactions$576,135
R37 · FY2010 · GM · contact PI
Asymmetric Nucleophilic Catalysis$449,760
R01 · FY2010 · GM · contact PI
Asymmetric Nucleophilic Catalysis$411,215
R01 · FY2010 · GM · contact PI
Asymmetric Nucleophilic Catalysis$363,707
R01 · FY2009 · GM · contact PI
Palladium- and Nickel-Catalyzed C-C Bond Formation$111,686
R01 · FY2009 · GM · contact PI
Palladium- and Nickel-Catalyzed C-C Bond Formation$480,797
R01 · FY2008 · GM · contact PI
Asymmetric Nucleophilic Catalysis$362,615
R01 · FY2008 · GM · contact PI
Palladium- and Nickel-Catalyzed C-C Bond Formation$480,732
R01 · FY2007 · GM · contact PI
Asymmetric Nucleophilic Catalysis$360,313
R01 · FY2007 · GM · contact PI
Palladium- and Nickel-Catalyzed C-C Bond Formation$480,672
R01 · FY2006 · GM · contact PI
Asymmetric Catalysis by Transition Metals$290,174
R01 · FY2006 · GM · contact PI
Asymmetric Nucleophilic Catalysis$240,439
R01 · FY2006 · GM · contact PI
Development of Enantioselective Nucleophilic Catalysts$128,604
R01 · FY2006 · GM · contact PI
Palladium- and Nickel-Catalyzed C-C Bond Formation$526,425
R01 · FY2005 · GM
Development of Enantioselective Nucleophilic Catalysts$373,608
R01 · FY2005 · GM
Asymmetric Catalysis by Transition Metals$297,504
R01 · FY2005 · GM
Development of Enantioselective Nucleophilic Catalysts$76,130
R01 · FY2005 · GM
Development of Enantioselective Nucleophilic Catalysts$380,955
R01 · FY2004 · GM
Asymmetric Catalysis by Transition Metals$297,837
R01 · FY2004 · GM
Versatile Methods for Palladium-Catalyzed Couplings$279,511
R01 · FY2004 · GM
Development of Enantioselective Nucleophilic Catalysts$29,830
R01 · FY2004 · GM
Development of Enantioselective Nucleophilic Catalysts$405,072
R01 · FY2003 · GM
Asymmetric Catalysis by Transition Metals$316,485
R01 · FY2003 · GM
Versatile Methods for Palladium-Catalyzed Couplings$279,511
R01 · FY2003 · GM
Development of Enantioselective Nucleophilic Catalysts$342,346
R01 · FY2002 · GM
Versatile Methods for Palladium-Catalyzed Couplings$279,511
R01 · FY2002 · GM
Development of Enantioselective Nucleophilic Catalysts$38,306
R01 · FY2002 · GM
Versatile Methods for Palladium-Catalyzed Couplings$299,778
R01 · FY2001 · GM
DEVELOPMENT OF ENANTIOSELECTIVE NUCLEOPHILIC CATALYSTS$282,338
R01 · FY2001 · GM
DEVELOPMENT OF ENANTIOSELECTIVE NUCLEOPHILIC CATALYSTS$232,938
R01 · FY2000 · GM
DEVELOPMENT OF ENANTIOSELECTIVE NUCLEOPHILIC CATALYSTS$26,672
R01 · FY2000 · GM