Evidence map›Paper›PMID 26358769›Full record

ArticleAngewandte Chemie (International ed. in English)2015

Rhodium(III)-Catalyzed Allylic C(sp(3))-H Activation of Alkenyl Sulfonamides: Unexpected Formation of Azabicycles.

Alexis Archambeau, Tomislav Rovis

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

2 authors.

Alexis ArchambeauDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523 (USA) http://sites.chem.colostate.edu/rovislab.
Tomislav RovisDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523 (USA) http://sites.chem.colostate.edu/rovislab. rovis@colostate.edu.

Funding

Asymmetric Synthesis of Nitrogen HeterocyclesR01GM080442 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ROVIS, TOMISLAV · 2007 to 2024
$5.5M
NIGMS NIH HHS GM80442NIGMS NIH HHS R01 GM080442
6 · The paper itself

Abstract

Unsaturated N-sulfonamides undergo a Rh(III)-catalyzed allylic C(sp(3))-H activation followed by insertion with an exogenous internal alkyne. The reaction generates [3.3.0], [4.3.0], and [5.3.0] azabicyclic structures with excellent diastereoselectivity. Deuterium labeling experiments implicate a 1,3-Rh shift as a key step in the mechanism.

Indexed as

AlkenesAlkynesAzabicyclo CompoundsCatalysisMolecular StructureOrganometallic CompoundsRhodiumSulfonamidesAlkenesAlkynesAzabicyclo CompoundsOrganometallic CompoundsRhodiumSulfonamides1,3-migration4π-electrocyclizationazabicyclesCH insertionrhodium

Identifiers

PMID26358769
PMCPMC4676418

What OpenQuestion holds

Textmetadata
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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.