Katsumasa Nakajima - Concepedia

Concepedia

Author

Katsumasa Nakajima

University of Calgary ORCID

Also Known As

K. NAKAJIMA, K. Nakajima, Katsumasa Nakajima, Nakajima, Katsumasa

44

Publications

1.1K

Citations

17

H-Index

39

Concepts

All Affiliations

University of Calgary Harvard University University of Delaware Novartis (Switzerland)Novartis Institutes for BioMedical Research

KN

About

Katsumasa Nakajima is an author at University of Calgary specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	9	9	507
2	Natural Sciences	6	6	441
3	Biochemistry	5	5	197
4	Medicine	3	3	285
5	Health Sciences	1	1	18

Katsumasa Nakajima

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17

Publications

1.1K

Citations

17

H-Index

	Year	Citations
Discovery of Orally Active Inhibitors of Brahma Homolog (BRM)/SMARCA2 ATPase Activity for the Treatment of Brahma Related Gene 1 (BRG1)/SMARCA4-Mutant Cancers Julien P. N. Papillon, Katsumasa Nakajima, Christopher D. Adair, Journal of Medicinal Chemistry Brahma HomologMolecular BiologyCancer BiologyTumor BiologyTranscriptional Regulation	2018	225
Asymmetric Ni(II)/Cr(II)-Mediated Coupling Reaction: Catalytic Process Hyeong-Wook Choi, Katsumasa Nakajima, Damtew Demeke, Organic Letters Inorganic ChemistryChemical EngineeringAsymmetric NiEngineeringCross-coupling Reaction	2002	120
Asymmetric Ni(II)/Cr(II)-Mediated Coupling Reaction: Stoichiometric Process Zhao‐Kui Wan, Hyeong-Wook Choi, Fu‐An Kang, Organic Letters	2002	92
A Convenient New Route to Piperidines, Pyrrolizidines, Indolizidines, and Quinolizidines by Cyclization of Acetylenic Sulfones with β- and γ-Chloroamines. Enantioselective Total Synthesis of Indolizidines<b>(</b><b>−</b><b>)-167B</b>,<b>(</b><b>−</b><b>)-209D</b>,<b>(</b><b>−</b><b>)-209B</b>, and<b>(</b><b>−</b><b>)-207A</b> Thomas G. Back, Katsumasa Nakajima The Journal of Organic Chemistry	2000	84
Silylmethylations of C60 with Grignard Reagents: Selective Synthesis of HC60CH2SiMe2Y and C60(CH2SiMe2Y)2 with Selection of Solvents Hideo Nagashima, Hiroshi Terasaki, Eiji Kimura, The Journal of Organic Chemistry HalogenationMolecular SciencesEngineeringGrignard ReagentsChemical Derivative	1994	76
Synthetic studies on the marine natural product halichondrins Hyeong-Wook Choi, Damtew Demeke, Fu‐An Kang, Pure and Applied Chemistry Bioorganic ChemistryEngineeringOrganic ChemistryChemistryCrystalline Cr	2003	71
Tandem Conjugate Additions and 3-Aza-Cope Rearrangements of Tertiary Allyl Amines and Cyclic α-Vinylamines with Acetylenic Sulfones. Applications to Simple and Iterative Ring Expansions Leading to Medium and Large-Ring Nitrogen Heterocycles Mitchell H. Weston, Katsumasa Nakajima, Thomas G. Back The Journal of Organic Chemistry Cross-coupling ReactionEnantioselective SynthesisZwitterion IntermediatesEngineeringAlkene Metathesis	2008	63
Enantioselective Synthesis of (−)-Pumiliotoxin C from a Chiral Amino Ester and an Acetylenic Sulfone that Acts as an Alkene Dipole Equivalent Thomas G. Back, Katsumasa Nakajima The Journal of Organic Chemistry EngineeringPig Liver EsteraseOrganic ChemistryCurtius RearrangementDiversity Oriented Synthesis	1998	56
Identification of a PCSK9-LDLR disruptor peptide with in vivo function Margaret E. Brousseau, Kevin B. Clairmont, Glen Spraggon, Cell chemical biology InflammationSignal TransductionPeptide LibraryImmunologyPcsk9-ldlr Disruptor Peptide	2021	42
The Discovery of SWI/SNF Chromatin Remodeling Activity as a Novel and Targetable Dependency in Uveal Melanoma Florencia Rago, GiNell Elliott, Ailing Li, Molecular Cancer Therapeutics	2020	38

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