Evidence map›Paper›PMID 20873839›Full record

ArticleAccounts of chemical research2010

Mechanistically driven development of iridium catalysts for asymmetric allylic substitution.

John F Hartwig, Levi M Stanley

Abstract read
In one paragraph

Article in Accounts of chemical research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

101 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Iridium-Catalyzed Stereocontrolled C(spJournal of the American Chemical Society · 2025
    Article
  11. Review
  12. Asymmetric Amination of Unstrained C(spJournal of the American Chemical Society · 2024
    Article
  13. Article
  14. Article
  15. Simultaneous Stereoinvertive and Stereoselective C(spJournal of the American Chemical Society · 2024
    Article
  16. Article
  17. Asymmetric α-C(spNature communications · 2024
    Article
  18. Review
  19. Article
  20. Review

41 more citing papers are in PubMed but not listed here.

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.

John F HartwigDepartment of Chemistry, University of Illinois, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
Levi M Stanley

Funding

RATIONAL DESIGN OF CATALYSTS FOR C-C BOND FORMATIONR01GM058108 · NIGMS · YALE UNIVERSITY · PI HARTWIG, JOHN F · 1999 to 2014
$5.1M
Mechanism and Development of Catalysts for the Synthesis of Amines, Ethers, and SR37GM055382 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI HARTWIG, JOHN F · 2009 to 2018
$4.4M
TRANSITION METAL-CATALYZED SYNTHESIS OF AMINES AND ETHERR01GM055382 · NIGMS · YALE UNIVERSITY · PI HARTWIG, JOHN F · 2001 to 2008
$2.5M
PALLADIUM CATALYZED FORMATION OF ARYLAMINE AND ARYLETHERR29GM055382 · NIGMS · YALE UNIVERSITY · PI HARTWIG, JOHN F · 1997 to 2000
$185k
Transition Metal-Catalyzed, Asymmetric Allylic Borylation and SilylationF32GM084584 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI STANLEY, LEVI MICHAEL · 2008 to 2010
$129k
NIGMS NIH HHS F32 GM084584NIGMS NIH HHS GM-55382NIGMS NIH HHS GM-58108NIGMS NIH HHS GM-84584NIGMS NIH HHS R01 GM055382NIGMS NIH HHS R01 GM058108NIGMS NIH HHS R29 GM055382NIGMS NIH HHS R37 GM055382
6 · The paper itself

Abstract

Enantioselective allylic substitution reactions comprise some of the most versatile methods for preparing enantiomerically enriched materials. These reactions form products that contain multiple functionalities by creating carbon-nitrogen, carbon-oxygen, carbon-carbon, and carbon-sulfur bonds. For many years, the development of catalysts for allylic substitution focused on palladium complexes. However, studies of complexes of other metals have revealed selectivities that often complement those of palladium systems. Most striking is the observation that reactions with unsymmetrical allylic electrophiles that typically occur with palladium catalysts at the less hindered site of an allylic electrophile occur at the more hindered site with catalysts based on other metals. In this Account, we describe the combination of an iridium precursor and a phosphoramidite ligand that catalyzes enantioselective allylic substitution reactions with a particularly broad scope of nucleophiles. The active form of this iridium catalyst is not generated by the simple binding of the phosphoramidite ligand to the metal precursor. Instead, the initial phosphoramidite and iridium precursor react in the presence of base to form a metallacyclic species that is the active catalyst. This species is generated either in situ or separately in isolated form by reactions with added base. The identification of the structure of the active catalyst led to the development of simplified catalysts as well as the most active form of the catalyst now available, which is stabilized by a loosely bound ethylene. Most recently, this structure was used to prepare intermediates containing allyl ligands, the structures of which provide a model for the enantioselectivities discussed here. Initial studies from our laboratory on the scope of iridium-catalyzed allylic substitution showed that reactions of primary and secondary amines, including alkylamines, benzylamines, and allylamines, and reactions of phenoxides and alkoxides occurred in high yields, with high branched-to-linear ratios and high enantioselectivities. Parallel mechanistic studies had revealed the metallacyclic structure of the active catalyst, and subsequent experiments with the purposefully formed metallacycle increased the reaction scope dramatically. Aromatic amines, azoles, ammonia, and amides and carbamates as ammonia equivalents all reacted with high selectivities and yields. Moreover, weakly basic enolates (such as silyl enol ethers) and enolate equivalents (such as enamines) also reacted, and other research groups have used this catalyst to conduct reactions of stabilized carbon nucleophiles in the absence of additional base. One hallmark of the reactions catalyzed by this iridium system is the invariably high enantioselectivity, which reflects a high stereoselectivity for formation of the allyl intermediate. Enantioselectivity typically exceeds 95%, regioselectivity for formation of branched over linear products is usually near 20:1, and yields generally exceed 75% and are often greater than 90%. Thus, the development of iridium catalysts for enantioselective allylic substitution shows how studies of reaction mechanism can lead to a particularly active and a remarkably general system for an enantioselective process. In this case, a readily accessible catalyst effects allylic substitution, with high enantioselectivity and regioselectivity complementary to that of the venerable palladium systems.

Indexed as

CatalysisHydrocarbonsIridiumMolecular StructurePalladiumRhodiumHydrocarbonsIridiumPalladiumRhodium

Identifiers

PMID20873839
PMCPMC3008324

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