Evidence map›Paper›PMID 34354327›Full record

ArticleSynlett : accounts and rapid communications in synthetic organic chemistry2021

Harnessing C-O Bonds in Stereoselective Cross-Coupling and Cross-Electrophile Coupling Reactions.

Amberly B Sanford, Elizabeth R Jarvo

Abstract read
In one paragraph

Article in Synlett : accounts and rapid communications in synthetic organic chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amberly B SanfordDepartment of Chemistry, University of California, Irvine Natural Sciences II, Irvine, CA, 92697-2025.
Elizabeth R JarvoDepartment of Chemistry, University of California, Irvine Natural Sciences II, Irvine, CA, 92697-2025.

Funding

Stereospecific Nickel-Catalyzed Cross-Coupling for Pharmacophore SynthesisR01GM100212 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI JARVO, ELIZABETH REINHARDT · 2012 to 2016
$1.4M
NIGMS NIH HHS R01 GM100212
6 · The paper itself

Abstract

Herein, we discuss our laboratory's research in the activation of alcohol derivatives in cross-coupling and cross-electrophile coupling reactions. Our developed methods enable the use of secondary alcohols to afford tertiary stereogenic centers, which we applied to the synthesis of pharmaceutically relevant compounds and substructures. We first discuss the synthesis of bioactive compounds via stereospecific Kumada cross-coupling reactions, followed by a discussion on the development of our stereoselective cross-electrophile coupling reaction to synthesize cyclopropanes.

Indexed as

asymmetric synthesiscross-couplingcross-electrophile couplingenantioselective synthesisnickel

Identifiers

PMID34354327
PMCPMC8329764

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Registered trials

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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.