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 93 Citations 22,691 363 World Ranking 1023 National Ranking 437

Research.com Recognitions

Awards & Achievements

2017 - Fellow of the American Association for the Advancement of Science (AAAS)

2003 - Fellow of Alfred P. Sloan Foundation

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

His main research concerns Catalysis, Organic chemistry, Transfer hydrogenation, Aldehyde and Enantioselective synthesis. His Catalysis research integrates issues from Reagent and Medicinal chemistry. His research on Organic chemistry frequently links to adjacent areas such as Polymer chemistry.

In Transfer hydrogenation, Michael J. Krische works on issues like Alcohol oxidation, which are connected to Nucleophile. As part of the same scientific family, he usually focuses on Aldehyde, concentrating on Alcohol and intersecting with Isotopic labeling and Redox. His biological study spans a wide range of topics, including Dehydrogenation, Allyl acetate and Stereochemistry.

His most cited work include:

  • Interconversion of single and double helices formed from synthetic molecular strands (482 citations)
  • Transition Metal Catalyzed Cycloisomerizations (298 citations)
  • Formation of C–C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation (247 citations)

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

Michael J. Krische mainly focuses on Catalysis, Organic chemistry, Enantioselective synthesis, Medicinal chemistry and Transfer hydrogenation. His work in Catalysis covers topics such as Combinatorial chemistry which are related to areas like Nucleophile. His Enantioselective synthesis research includes themes of Allyl acetate and Stereochemistry.

His studies deal with areas such as Hydrogen, Oxidative coupling of methane, Regioselectivity and Phosphine as well as Medicinal chemistry. His work deals with themes such as Alcohol oxidation, Dehydrogenation, Hydroformylation, Redox and Allyl compound, which intersect with Transfer hydrogenation. His studies in Aldehyde integrate themes in fields like Alcohol and Electrophile.

He most often published in these fields:

  • Catalysis (67.77%)
  • Organic chemistry (45.04%)
  • Enantioselective synthesis (29.75%)

What were the highlights of his more recent work (between 2015-2021)?

  • Catalysis (67.77%)
  • Enantioselective synthesis (29.75%)
  • Organic chemistry (45.04%)

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

Michael J. Krische mainly investigates Catalysis, Enantioselective synthesis, Organic chemistry, Ruthenium and Medicinal chemistry. His Catalysis research is multidisciplinary, relying on both Combinatorial chemistry and Stereochemistry. The Enantioselective synthesis study combines topics in areas such as Alcohol, Total synthesis, Allylic rearrangement and Dehydrogenation.

His Ruthenium study also includes fields such as

  • Ring which is related to area like Diastereomer,
  • Polymer chemistry together with Phenylene. He studied Medicinal chemistry and Enyne that intersect with BINAP. His research integrates issues of SEGPHOS, Allyl acetate, Aldehyde and Allyl compound in his study of Iridium.

Between 2015 and 2021, his most popular works were:

  • Intermolecular Metal-Catalyzed Reductive Coupling of Dienes, Allenes, and Enynes with Carbonyl Compounds and Imines. (117 citations)
  • Metal-catalyzed reductive coupling of olefin-derived nucleophiles: Reinventing carbonyl addition (107 citations)
  • Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis (106 citations)

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

  • Organic chemistry
  • Catalysis
  • Alkene

Michael J. Krische mostly deals with Catalysis, Enantioselective synthesis, Organic chemistry, Transfer hydrogenation and Stereochemistry. Michael J. Krische has researched Catalysis in several fields, including Reagent, Redox and Medicinal chemistry. The various areas that Michael J. Krische examines in his Enantioselective synthesis study include Methanol, Stereoisomerism, Allylic rearrangement, Carbonylation and Iridium.

His Transfer hydrogenation research is multidisciplinary, incorporating perspectives in Rhodium and Imine. The study incorporates disciplines such as Hydrogen and Carbon in addition to Stereochemistry. Michael J. Krische combines subjects such as Primary alcohol and Aldehyde with his study of Dehydrogenation.

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

Interconversion of single and double helices formed from synthetic molecular strands

Volker Berl;Ivan Huc;Richard G. Khoury;Michael J Krische.
Nature (2000)

701 Citations

Supramolecular Polymers Generated from Heterocomplementary Monomers Linked through Multiple Hydrogen-Bonding Arrays—Formation, Characterization, and Properties

Volker Berl;Marc Schmutz;Michael J. Krische;Richard G. Khoury.
Chemistry: A European Journal (2002)

386 Citations

Enantioselective C-H Crotylation of Primary Alcohols via Hydrohydroxyalkylation of Butadiene

Jason R. Zbieg;Eiji Yamaguchi;Emma L. McInturff;Michael J. Krische.
Science (2012)

384 Citations

Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: Borrowing hydrogen, returning carbon

John M. Ketcham;Inji Shin;T. Patrick Montgomery;Michael J. Krische.
Angewandte Chemie (2014)

352 Citations

Transition Metal Catalyzed Cycloisomerizations

Barry M. Trost;Michael J. Krische.
Synlett (1998)

334 Citations

Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones via rhodium-catalyzed asymmetric hydrogenation: mechanistic insight into the role of Brønsted acid additives.

Venukrishnan Komanduri;Michael J Krische.
Journal of the American Chemical Society (2006)

320 Citations

Enantioselective Iridium Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level via Transfer Hydrogenative Coupling of Allyl Acetate: Departure from Chirally Modified Allyl Metal Reagents in Carbonyl Addition

In Su Kim;Ming Yu Ngai;Michael J Krische.
Journal of the American Chemical Society (2008)

317 Citations

Intermolecular Metal-Catalyzed Reductive Coupling of Dienes, Allenes, and Enynes with Carbonyl Compounds and Imines.

Michael Holmes;Leyah A. Schwartz;Michael J. Krische.
Chemical Reviews (2018)

302 Citations

Catalytic Carbonyl Addition through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents

John F. Bower;In Su Kim;Ryan L. Patman;Michael J. Krische.
Angewandte Chemie (2009)

263 Citations

Organocatalytic Michael cycloisomerization of bis(enones): the intramolecular Rauhut-Currier reaction.

Long Cheng Wang;Ana Liza Luis;Kyriacos Agapiou;Hye Young Jang.
Journal of the American Chemical Society (2002)

260 Citations

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