Evidence map›Paper›PMID 26703561›Full record

ReviewMolecules (Basel, Switzerland)2015

Isocyanide-Based Multicomponent Reactions for the Synthesis of Heterocycles.

András Váradi, Travis C Palmer, Rebecca Notis Dardashti, Susruta Majumdar

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Multicomponent Reactions for the Synthesis of Oxazepines.Topics in current chemistry (Cham) · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Ugi Four-Component Reactions Using Alternative Reactants.Molecules (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Three-Component Reactions of 3-Arylidene-3Molecules (Basel, Switzerland) · 2021
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Al(Salen) Metal Complexes in Stereoselective Catalysis.Molecules (Basel, Switzerland) · 2019
    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

4 authors.

András VáradiDepartment of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. varadia@mskcc.org.
Travis C PalmerDepartment of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. palmertr@grinnell.edu.
Rebecca Notis DardashtiDepartment of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. rebecca.dardashti@mail.huji.ac.il.
Susruta MajumdarDepartment of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. majumdas@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Analgesics targeting truncated 6transmembrane exon 11 variants of MOR-1 (6TM-E11)R33DA034106 · NIDA · SLOAN-KETTERING INST CAN RESEARCH · PI MAJUMDAR, SUSRUTA · 2014 to 2015
$596k
Analgesics targeting truncated 6transmembrane exon 11 variants of MOR-1 (6TM-E11)R21DA034106 · NIDA · SLOAN-KETTERING INST CAN RESEARCH · PI MAJUMDAR, SUSRUTA · 2012 to 2013
$443k
NCI NIH HHS P30 CA008748NIDA NIH HHS DA034106NIDA NIH HHS R21 DA034106NIDA NIH HHS R33 DA034106
6 · The paper itself

Abstract

Multicomponent reactions (MCRs) are extremely popular owing to their facile execution, high atom-efficiency and the high diversity of products. MCRs can be used to access various heterocycles and highly functionalized scaffolds, and thus have been invaluable tools in total synthesis, drug discovery and bioconjugation. Traditional isocyanide-based MCRs utilize an external nucleophile attacking the reactive nitrilium ion, the key intermediate formed in the reaction of the imine and the isocyanide. However, when reactants with multiple nucleophilic groups (bisfunctional reactants) are used in the MCR, the nitrilium intermediate can be trapped by an intramolecular nucleophilic attack to form various heterocycles. The implications of nitrilium trapping along with widely applied conventional isocyanide-based MCRs in drug design are discussed in this review.

Indexed as

Combinatorial Chemistry TechniquesCyanidesHeterocyclic CompoundsIminesMolecular StructureStructure-Activity RelationshipCyanidesHeterocyclic CompoundsIminesheterocyclesnitrilium trappingUgi reaction

Identifiers

PMID26703561
PMCPMC4782750

What OpenQuestion holds

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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.