Evidence map›Paper›PMID 40837102›Full record

ArticleACS catalysis2024

Rh(III)-Catalyzed Alkene

Noah Wagner-Carlberg, Julia R Dorsheimer, Tomislav Rovis

Abstract read
In one paragraph

Article in ACS catalysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Noah Wagner-CarlbergDepartment of Chemistry, Columbia University, New York, New York 10027, United States.
Julia R DorsheimerDepartment of Chemistry, Columbia University, New York, New York 10027, United States.
Tomislav RovisDepartment of Chemistry, Columbia University, New York, New York 10027, United States.

Funding

Asymmetric Synthesis of Nitrogen HeterocyclesR01GM080442 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ROVIS, TOMISLAV · 2007 to 2024
$5.5M
Cryoprobe Upgrade of a 500 MHz NMR SpectrometerS10OD026749 · OD · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DECATUR, JOHN D · 2019 to 2019
$376k
NIGMS NIH HHS R01 GM080442NIH HHS S10 OD026749
6 · The paper itself

Abstract

Alkene difunctionalization methods are an attractive way to rapidly build molecular complexity using readily available starting materials. One common approach is transition metal-catalyzed nucleometalation, which converts the C-C double bond to a C-Nu bond and a C-M bond. Commonly, a tethered nucleophile is used in order to form pharmaceutically relevant heterocyclic cores in this manner. The resulting alkylmetal species can then be further functionalized in a number of ways. While methods exist to aminate the C-M bond, direct installation of valuable amides is rare. Additionally, nucleometalation methods are often limited to the use of a single type of nucleophile. Herein we disclose a general method for the Rh(III)-catalyzed nucleoamidation of alkenes, forming a variety of heterocyclic cores.

Indexed as

alkene difunctionalizationamidationanti additionheterocyclesrhodium

Identifiers

PMID40837102
PMCPMC12363399

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.