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Jeffrey Nicholas Johnston

Indiana University Bloomington

$11,251,553
Attributed
$11,251,553
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 $1.2M · FY200525
$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$11,251,553 · 6

By mechanism

R01$10,537,334 · 4
R35$422,569 · 1
R56$291,650 · 1

Top collaborators

No co-investigators on record.

Others in their field

Top investigators on “Small Molecule

Research focus

Small MoleculeChemical SynthesisBaseProgramsAminesReactionCarbonComplexReagentMediatingCostNitroalkaneAmino AcidsEnantiomerTherapeutic DevelopmentInnovationVariantCatalysisBiological FactorsStereoisomerIonsNatural ProductsMetalsNames

Grant awards (31)

Development of Mirror-Image Natural Products as Antiarrhythmic Therapeutics$744,145
R01 · FY2025 · HL · contact PI
New Methods for Therapeutic Development$422,569
R35 · FY2025 · GM · contact PI
Development of a Mirror-Image Natural Product as an Antiarrhythmic Therapeutic$768,804
R01 · FY2023 · HL · contact PI
Development of a Mirror-Image Natural Product as an Antiarrhythmic Therapeutic$777,069
R01 · FY2022 · HL · contact PI
Studies in Amide and Peptide Synthesis$343,741
R01 · FY2022 · GM · contact PI
Development of a Mirror-Image Natural Product as an Antiarrhythmic Therapeutic$784,438
R01 · FY2021 · HL · contact PI
Studies in Amide and Peptide Synthesis$343,922
R01 · FY2021 · GM · contact PI
Development of a Mirror-Image Natural Product as an Antiarrhythmic Therapeutic$787,474
R01 · FY2020 · HL · contact PI
Studies in Amide and Peptide Synthesis$344,100
R01 · FY2020 · GM · contact PI
Studies in Amide and Peptide Synthesis$344,275
R01 · FY2019 · GM · contact PI
Enantioselective Functionalizations of Azomethines and Alkenes$284,639
R01 · FY2017 · GM · contact PI
Enantioselective Functionalizations of Azomethines and Alkenes$284,907
R01 · FY2016 · GM · contact PI
Studies in Amide and Peptide Synthesis$327,802
R01 · FY2015 · GM · contact PI
Enantioselective Functionalizations of Azomethines and Alkenes$278,001
R01 · FY2015 · GM · contact PI
Studies in Amide and Peptide Synthesis$328,102
R01 · FY2014 · GM · contact PI
Enantioselective Functionalizations of Azomethines and Alkenes$278,399
R01 · FY2014 · GM · contact PI
Studies in Amide and Peptide Synthesis$316,901
R01 · FY2013 · GM · contact PI
Studies in Amide and Peptide Synthesis$328,683
R01 · FY2012 · GM · contact PI
New Stereoselective Reactions for Chiral Amine Synthesis$253,478
R01 · FY2012 · GM · contact PI
New Stereoselective Reactions for Chiral Amine Synthesis$254,459
R01 · FY2011 · GM · contact PI
Application of New Amination Reactions to Natural Product and Nonnatural Heterocy$314,317
R01 · FY2010 · GM · contact PI
New Stereoselective Reactions for Chiral Amine Synthesis$257,963
R01 · FY2010 · GM · contact PI
Application of New Amination Reactions to Natural Product and Nonnatural Heterocy$314,161
R01 · FY2009 · GM · contact PI
New Stereoselective Reactions for Chiral Amine Synthesis$261,459
R01 · FY2009 · GM · contact PI
Application of New Amination Reactions to Natural Product and Nonnatural Heterocy$291,650
R56 · FY2008 · GM · contact PI
New Aryl and Vinyl Amination Methods$250,373
R01 · FY2006 · GM · contact PI
New Aryl and Vinyl Amination Methods$144,145
R01 · FY2005 · GM
New Aryl and Vinyl Amination Methods$103,509
R01 · FY2005 · GM
New Aryl and Vinyl Amination Methods$245,274
R01 · FY2004 · GM
New Aryl and Vinyl Amination Methods$245,515
R01 · FY2003 · GM
New Aryl and Vinyl Amination Methods$227,279
R01 · FY2002 · GM