D-Index & Metrics

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 42 Citations 7,069 247 World Ranking 13992 National Ranking 1056

Research.com Recognitions

Awards & Achievements

1984 - Liebig-Denkmünze (Liebig Medal), Society of German Chemists

Overview

What is he best known for?

The fields of study Ulrich Schöllkopf is best known for:

  • Organic chemistry
  • Ketone
  • Catalysis

Ulrich Schöllkopf integrates Organic chemistry and Combinatorial chemistry in his research. His work often combines Combinatorial chemistry and Organic chemistry studies. While working in this field, he studies both Stereochemistry and Enantioselective synthesis. His study ties his expertise on Biochemistry together with the subject of Enantioselective synthesis. He conducts interdisciplinary study in the fields of Biochemistry and Amino acid through his works. He merges Amino acid with Stereochemistry in his study. His Catalysis study often links to related topics such as Oxazoline. The study of Medicinal chemistry is intertwined with the study of Butyllithium in a number of ways. Butyllithium connects with themes related to Medicinal chemistry in his study.

His most cited work include:

  • Über Triphenyl‐phosphin‐methylene als olefinbildende Reagenzien (I. Mitteil. (843 citations)
  • Enantioselective Syntheses of(R)-Amino Acids UsingL-Valine as Chiral Agent (232 citations)
  • Enantioselective synthesis of non-proteinogenic amino acids via metallated bis-lactim ethers of 2,5-diketopiperazines (183 citations)

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

Ulrich Schöllkopf merges many fields, such as Organic chemistry and Combinatorial chemistry, in his writings. Ulrich Schöllkopf undertakes multidisciplinary studies into Combinatorial chemistry and Organic chemistry in his work. Ulrich Schöllkopf performs multidisciplinary studies into Stereochemistry and Enantioselective synthesis in his work. He merges Enantioselective synthesis with Stereochemistry in his research. Ulrich Schöllkopf undertakes multidisciplinary studies into Catalysis and Ether in his work. He combines Ether and Catalysis in his research. Ulrich Schöllkopf incorporates Biochemistry and Amino acid in his studies. In his works, he performs multidisciplinary study on Amino acid and Biochemistry.

Ulrich Schöllkopf most often published in these fields:

  • Organic chemistry (61.88%)
  • Stereochemistry (48.75%)
  • Medicinal chemistry (46.88%)

What were the highlights of his more recent work (between 1989-1993)?

  • Stereochemistry (100.00%)
  • Organic chemistry (100.00%)
  • Catalysis (75.00%)

In recent works Ulrich Schöllkopf was focusing on the following fields of study:

Ulrich Schöllkopf combines Stereochemistry and Enantiomer in his research. In his study, he carries out multidisciplinary Enantiomer and Stereochemistry research. In his works, he performs multidisciplinary study on Organic chemistry and Combinatorial chemistry. He incorporates Combinatorial chemistry and Organic chemistry in his research. He conducts interdisciplinary study in the fields of Catalysis and Cyclopentadiene through his research. Ulrich Schöllkopf merges Ether with Alkyl in his research. In his work, he performs multidisciplinary research in Alkyl and Carboxylic acid. His work blends Carboxylic acid and Ether studies together. In his research, he undertakes multidisciplinary study on Enantioselective synthesis and Diastereomer.

Between 1989 and 1993, his most popular works were:

  • Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline (55 citations)
  • Asymmetric synthesis of diastereomerically and enantiomerically pure α-amino-γ-nitro carboxylic esters via Michael addition of the titanated bislactim ether of cyclo (-L-Val-Gly-) to nitroolefines (47 citations)
  • Asymmetric Syntheses via Heterocyclic Intermediates, XLV. Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-serine Methyl Esters (35 citations)

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.

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