His primary areas of investigation include Organic chemistry, Adduct, Medicinal chemistry, Palladium and Regioselectivity. His study in Adduct is interdisciplinary in nature, drawing from both Friedel–Crafts reaction, Michael reaction, Intramolecular force, Stereochemistry and Trifluoroacetic acid. His Medicinal chemistry study incorporates themes from Quinoline, Baylis–Hillman reaction, Derivative, Chemical transformation and Aryl.
He interconnects Indole test, Electrophilic addition and Deprotonation in the investigation of issues within Palladium. His biological study spans a wide range of topics, including Pyrazole, Hydrazine, Sulfur and Ylide. His Catalysis study deals with Combinatorial chemistry intersecting with Nitrile and Chelation.
His primary areas of study are Organic chemistry, Medicinal chemistry, Adduct, Catalysis and Regioselectivity. His research on Organic chemistry frequently connects to adjacent areas such as Ninhydrin. His studies in Medicinal chemistry integrate themes in fields like Yield, Moiety, Aryl, Intramolecular force and Nucleophile.
The study incorporates disciplines such as Annulation, Michael reaction, Stereochemistry, Radical cyclization and Isomerization in addition to Adduct. Jae Nyoung Kim studies Palladium which is a part of Catalysis.
Jae Nyoung Kim spends much of his time researching Medicinal chemistry, Organic chemistry, Adduct, Intramolecular force and Catalysis. The various areas that he examines in his Medicinal chemistry study include Bromide, Allylic rearrangement, Regioselectivity and Alkyl. His research links Oxidative phosphorylation with Organic chemistry.
His work in Adduct addresses subjects such as Ring, which are connected to disciplines such as Aromatization and Domino. Jae Nyoung Kim combines subjects such as Friedel–Crafts reaction, Oxidative coupling of methane and One-pot synthesis with his study of Intramolecular force. His research in Catalysis intersects with topics in Benzene and Montmorillonite.
His primary areas of study are Medicinal chemistry, Organic chemistry, Adduct, Catalysis and Intramolecular force. His Medicinal chemistry research is multidisciplinary, incorporating elements of One-pot synthesis, Aryl, Oxidative phosphorylation and Stereoselectivity. In his articles, Jae Nyoung Kim combines various disciplines, including Organic chemistry and Immune modulator.
His Adduct research includes elements of Ring, Phosphorus, Stereochemistry and Regioselectivity. Palladium is the focus of his Catalysis research. His Intramolecular force research integrates issues from Friedel–Crafts reaction, Alkene, Methanesulfonic acid and Ylide.
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Regioselective synthesis of 1,3,4,5-tetrasubstituted pyrazoles from Baylis–Hillman adducts
Ka Young Lee;Jeong Mi Kim;Jae Nyoung Kim.
Tetrahedron Letters (2003)
Baylis-Hillman reaction and chemical transformations of Baylis-Hillman adducts
Ka Young Lee;Saravanan Gowrisankar;Jae Nyoung Kim.
Bulletin of The Korean Chemical Society (2005)
Recent advances in the Pd-catalyzed chemical transformations of Baylis–Hillman adducts
Saravanan Gowrisankar;Hyun Seung Lee;Sung Hwan Kim;Ka Young Lee.
Tetrahedron (2009)
Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines
Jae Nyoung Kim;Hong Jung Lee;Ka Young Lee;Hyoung Shik Kim.
Tetrahedron Letters (2001)
Synthesis of enantiomerically enriched Baylis–Hillman alcohols from their acetates: combination of kinetic resolution during the salt formation with (DHQD)2PHAL and following asymmetric induction during hydrolysis with NaHCO3 as a water surrogate
Jae Nyoung Kim;Hong Jung Lee;Ji Hyeon Gong.
Tetrahedron Letters (2002)
Synthesis of N-substituted 1,4-dihydroquinolines from the Baylis–Hillman acetates via the successive SN2′–SNAr isomerization strategy
Jae Nyoung Kim;Hyoung Shik Kim;Ji Hyeon Gong;Yun Mi Chung.
Tetrahedron Letters (2001)
Synthesis of 3-ethoxycarbonyl-4-hydroxyquinoline N-oxides from the Baylis-Hillman adducts of o-nitrobenzaldehydes
Jae Nyoung Kim;Ka Young Lee;Hyoung Shik Kim;Tae Yi Kim.
Organic Letters (2000)
Facile synthesis of 2H-indazole derivatives starting from the Baylis–Hillman adducts of 2-cyclohexen-1-one
Ka Young Lee;Saravanan Gowrisankar;Jae Nyoung Kim.
Tetrahedron Letters (2005)
Synthesis of quinolines from the Baylis–Hillman acetates via the oxidative cyclization of sulfonamidyl radical as the key step
Jae Nyoung Kim;Yun Mi Chung;Yang Jin Im.
Tetrahedron Letters (2002)
Highly efficient Pd-catalyzed synthesis of nitriles from aldoximes
Hoo Sook Kim;Sung Hwan Kim;Jae Nyoung Kim.
Tetrahedron Letters (2009)
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