Evidence map›Paper›PMID 24720633›Full record

ArticleThe Journal of organic chemistry2014

Evolution of catalytic stereoselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity.

Amir H Hoveyda

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Rotaxane synthesisRSC advances · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. B(COrganometallics · 2024
    Article
  9. Article
  10. Synthesis ofJournal of the American Chemical Society · 2024
    Article
  11. Article
  12. Review
  13. Journal of the American Chemical Society · 2023
    Article
  14. Atroposelective Arene-Forming Alkene Metathesis.Angewandte Chemie (International ed. in English) · 2022
    Article
  15. Review
  16. The Ascent of Alkyne Metathesis to Strategy-Level Status.Journal of the American Chemical Society · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

1 author.

Amir H HoveydaDepartment of Chemistry, Merkert Chemistry Center, Boston College , Chestnut Hill, Massachusetts 02467, United States.

Funding

Catalytic Stereoselective Olefin Metathesis ReactionsR01GM059426 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HOVEYDA, AMIR H, SCHROCK, RICHARD R · 2000 to 2019
$10.0M
Catalytic and Stereoselective C-C Bond Forming ReactionsR37GM047480 · NIGMS · BOSTON COLLEGE · PI HOVEYDA, AMIR H · 2005 to 2014
$3.4M
CATALYTIC AND STEREOSELECTIVE C-C BOND FORMING REACTIONSR01GM047480 · NIGMS · BOSTON COLLEGE · PI HOVEYDA, AMIR H · 1997 to 2018
$2.6M
CATALYTIC &STEREOSELECTIVE C-C BOND FORMING REACTIONSR29GM047480 · NIGMS · BOSTON COLLEGE · PI HOVEYDA, AMIR H · 1992 to 1996
–
NIGMS NIH HHS GM-47480NIGMS NIH HHS GM-59426NIGMS NIH HHS R01 GM047480NIGMS NIH HHS R01 GM059426NIGMS NIH HHS R37 GM047480
6 · The paper itself

Abstract

There have been numerous significant advances in catalytic olefin metathesis (OM) during the past two decades. Such progress has transformed this important set of reactions to strategically pivotal processes that generate stereochemical identity while delivering molecules that cannot be easily prepared by alternative routes. In this Perspective, an analysis of the origin of the inception of bidentate benzylidene ligands for Ru-based OM catalysts is first presented. This is followed by an overview of the intellectual basis that culminated in the development of Mo-based diolates and stereogenic-at-Ru complexes for enantioselective OM. The principles accrued from the study of the latter Ru carbenes and Mo alkylidenes and utilized in the design of stereogenic-at-Mo, -W, and -Ru species applicable to enantioselective and Z-selective OM are then discussed. The influence of the recently introduced catalytic OM protocols on the design of synthesis routes leading to complex organic molecules is probed. The impact of a better understanding of the mechanistic nuances of OM toward the discovery of stereoselective catalysts is reviewed as well.

Indexed as

AlkenesBenzylidene CompoundsCatalysisLigandsMolecular StructureOrganometallic CompoundsRutheniumStereoisomerismAlkenesBenzylidene CompoundsLigandsOrganometallic CompoundsRuthenium

Identifiers

PMID24720633
PMCPMC4049245

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.