Evidence map›Paper›PMID 26200651›Full record

ArticleAccounts of chemical research2015

Advances in nickel-catalyzed cycloaddition reactions to construct carbocycles and heterocycles.

Ashish Thakur, Janis Louie

Abstract read
In one paragraph

Article in Accounts of chemical research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
  2. Rh-Catalyzed [2 + 2 + 2] Cycloaddition of Linked Bis(Diynes) Ar-C≡C-C≡C-(CHChemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  3. Preparation and Photochemistry of Hydroxy Isocyanate.The journal of physical chemistry. A · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Case Study of N-Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Nickel-Catalyzed Reductive [2+2] Cycloaddition of Alkynes.Journal of the American Chemical Society · 2018
    Article
  18. Bench-StableChemCatChem · 2018
    Article
  19. Air-Stable CpCoEuropean journal of organic chemistry · 2018
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ashish ThakurDepartment of Chemistry, University of Utah, 315 South, 1400 East, Salt Lake City, Utah 84112-0850, United States.
Janis LouieDepartment of Chemistry, University of Utah, 315 South, 1400 East, Salt Lake City, Utah 84112-0850, United States.

Funding

Transition Metal Mediated Routes to Heterocycles and CarbocyclesR01GM076125 · NIGMS · UNIVERSITY OF UTAH · PI LOUIE, JANIS · 2005 to 2017
$2.4M
NIGMS NIH HHS GM076125NIGMS NIH HHS R01 GM076125
6 · The paper itself

Abstract

Transition-metal catalysis has revolutionized the field of organic synthesis by facilitating the construction of complex organic molecules in a highly efficient manner. Although these catalysts are typically based on precious metals, researchers have made great strides in discovering new base metal catalysts over the past decade. This Account describes our efforts in this area and details the development of versatile Ni complexes that catalyze a variety of cycloaddition reactions to afford interesting carbocycles and heterocycles. First, we describe our early work in investigating the efficacy of N-heterocyclic carbene (NHC) ligands in Ni-catalyzed cycloaddition reactions with carbon dioxide and isocyanate. The use of sterically hindered, electron donating NHC ligands in these reactions significantly improved the substrate scope as well as reaction conditions in the syntheses of a variety of pyrones and pyridones. The high reactivity and versatility of these unique Ni(NHC) catalytic systems allowed us to develop unprecedented Ni-catalyzed cycloadditions that were unexplored due to the inefficacy of early Ni catalysts to promote hetero-oxidative coupling steps. We describe the development and mechanistic analysis of Ni/NHC catalysts that couple diynes and nitriles to form pyridines. Kinetic studies and stoichiometric reactions confirmed a hetero-oxidative coupling pathway associated with this Ni-catalyzed cycloaddition. We then describe a series of new substrates for Ni-catalyzed cycloaddition reactions such as vinylcyclopropanes, aldehydes, ketones, tropones, 3-azetidinones, and 3-oxetanones. In reactions with vinycyclopropanes and tropones, DFT calculations reveal noteworthy mechanistic steps such as a C-C σ-bond activation and an 8π-insertion of vinylcyclopropane and tropone, respectively. Similarly, the cycloaddition of 3-azetidinones and 3-oxetanones also requires Ni-catalyzed C-C σ-bond activation to form N- and O-containing heterocycles.

Indexed as

Carbon DioxideCatalysisCycloaddition ReactionCyclopropanesDiynesHeterocyclic CompoundsIsocyanatesKetonesMethaneNickelNitrilesPyridonesPyronesTropolonecarbeneCarbon DioxideCyclopropanesDiynesHeterocyclic CompoundsIsocyanatesKetonesMethaneNickelNitrilesPyridonesPyronesTropolonetropone

Identifiers

PMID26200651
PMCPMC6681814

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.