Evidence map›Paper›PMID 31535554›Full record

ArticleOrganic letters2019

Heterofunctionalized Cavitands by Macrocyclization of Sequence-Defined Foldamers.

Joseph W Meisel, Chunhua T Hu, Andrew D Hamilton

Abstract read
In one paragraph

Article in Organic letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

3 authors.

Joseph W MeiselDepartment of Chemistry , New York University , 100 Washington Square East , New York , New York 10003 , United States.ORCID 0000-0003-3348-0242
Chunhua T HuDepartment of Chemistry , New York University , 100 Washington Square East , New York , New York 10003 , United States.ORCID 0000-0002-8172-2202
Andrew D HamiltonDepartment of Chemistry , New York University , 100 Washington Square East , New York , New York 10003 , United States.

Funding

Peptidomimetics and Proteomimetics to Modulate Protein-Protein and Protein-Membrane InteractionsF32GM126851 · NIGMS · NEW YORK UNIVERSITY · PI MEISEL, JOSEPH W · 2017 to 2019
$168k
NIGMS NIH HHS F32 GM126851
6 · The paper itself

Abstract

Macrocyclic hosts have long been the workhorses of molecular recognition. Despite the widespread use of container-shaped molecules as synthetic receptors, an efficient preparation of cavitands bearing multiple functional groups has not been realized. This Letter describes a new cavitand derived from a sequence-defined oligoamide foldamer scaffold. A solid-phase synthesis approach is reported, which enables the display of multiple chemically diverse functional groups on the cavitand rim.

Indexed as

CyclizationEthers, CyclicMacrocyclic CompoundsMolecular StructureResorcinolsSolid-Phase Synthesis TechniquescavitandEthers, CyclicMacrocyclic CompoundsResorcinols

Identifiers

PMID31535554
PMCPMC6781098

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.