Evidence map›Paper›PMID 34334833›Full record

ArticleTetrahedron letters2021

Formation of Pyrroloindolines

Bhaskar D Joshi, John D Chisholm

Abstract read
In one paragraph

Article in Tetrahedron letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Bhaskar D JoshiDepartment of Chemistry, 1-014 Center for Science and Technology, Syracuse University, Syracuse, NY 13244.
John D ChisholmDepartment of Chemistry, 1-014 Center for Science and Technology, Syracuse University, Syracuse, NY 13244.

Funding

New Methods for the Synthesis of PyrroloindolinesR15GM116054 · NIGMS · SYRACUSE UNIVERSITY · PI CHISHOLM, JOHN DANIEL · 2015 to 2015
$318k
NIGMS NIH HHS R15 GM116054
6 · The paper itself

Abstract

Pyrroloindolines and related systems are present in a large number of complex natural products. These core structures have generated considerable synthetic interest, as many of the compounds possess challenging, elaborate structures and interesting biological properties. Recently we have focused on using trichloroacetimidates for the synthesis of these fascinating molecules. Trichloroacetimidates can be used as an electrophilic source of an alkyl group to form the pyrroloindoline directly from tryptamine derivatives. In this manner trichloroacetimidates provide a flexible solution to forming highly functionalized pyrroloindoline core structures, needing only a catalytic amount of a Lewis acid to effect the requisite transformations.

Indexed as

AlkylationHeterocyclePyrroloindolineTrichloroacetimidateTryptamine

Identifiers

PMID34334833
PMCPMC8321311

What OpenQuestion holds

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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.