D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 50 Citations 8,275 423 World Ranking 10663 National Ranking 190

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

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 most cited work include:

  • Regioselective synthesis of 1,3,4,5-tetrasubstituted pyrazoles from Baylis–Hillman adducts (182 citations)
  • Baylis-Hillman reaction and chemical transformations of Baylis-Hillman adducts (124 citations)
  • Recent advances in the Pd-catalyzed chemical transformations of Baylis–Hillman adducts (91 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Organic chemistry (53.63%)
  • Medicinal chemistry (36.56%)
  • Adduct (35.42%)

What were the highlights of his more recent work (between 2012-2021)?

  • Medicinal chemistry (36.56%)
  • Organic chemistry (53.63%)
  • Adduct (35.42%)

In recent papers he was focusing on the following fields of study:

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.

Between 2012 and 2021, his most popular works were:

  • 2,3‐Dichloro‐5,6‐dicyano‐para‐benzoquinone (DDQ)/Methanesulfonic Acid (MsOH)‐Mediated Intramolecular Arene‐Alkene Oxidative Coupling (43 citations)
  • An expedient synthesis of pyrrole-2-phosphonates via direct oxidative phosphorylation and γ-hydroxy-γ-butyrolactams from pyrroles (38 citations)
  • Palladium‐Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3‐(γ,δ‐Disubstituted)allylidene‐2‐Oxindoles (33 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Catalysis
  • Alkene

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

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)

289 Citations

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)

191 Citations

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)

140 Citations

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)

136 Citations

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)

115 Citations

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)

111 Citations

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)

106 Citations

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)

102 Citations

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)

97 Citations

Highly efficient Pd-catalyzed synthesis of nitriles from aldoximes

Hoo Sook Kim;Sung Hwan Kim;Jae Nyoung Kim.
Tetrahedron Letters (2009)

93 Citations

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