Evidence map›Paper›PMID 22622389›Full record

ArticleMolecular diversity2012

Applications of ortho-phenylisonitrile and ortho-N-Boc aniline for the two-step preparation of novel bis-heterocyclic chemotypes.

Zhigang Xu, Arthur Y Shaw, Gary S Nichol, Alexandra P Cappelli, Christopher Hulme

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

5 authors.

Zhigang XuCollege of Pharmacy, The University of Arizona, BIO5 Oro Valley, Oro Valley, AZ 85737, USA.
Arthur Y Shaw
Gary S Nichol
Alexandra P Cappelli
Christopher Hulme

Funding

The Southwest Comprehensive Center for Drug Discovery and DevelopmentRC2MH090878 · NIMH · TRANSLATIONAL GENOMICS RESEARCH INST · PI BERENS, MICHAEL E., HULME, CHRISTOPHER · 2009 to 2010
$7.6M
NIMH NIH HHS 5RC2 MH090878-02
6 · The paper itself

Abstract

Concise routes to five pharmacologically relevant bis-heterocyclic scaffolds are described. Significant molecular complexity is generated in a mere two synthetic operations enabling access to each scaffold. Routes are often improved by microwave irradiation and all utilize isocyanide-based multi-component reaction methods to incorporate the required diversity elements. Common reagents in all initial condensation reactions include 2-(N-Boc-amino)-phenyl-isocyanide 1, mono-Boc-phenylenediamine 2 and ethyl glyoxalate 3.

Indexed as

Aniline CompoundsCyclizationHeterocyclic CompoundsModels, MolecularMolecular ConformationNitrilesanilineAniline CompoundsHeterocyclic CompoundsNitriles

Identifiers

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.