Evidence map›Paper›PMID 28414243›Full record

ArticleJournal of the American Chemical Society2017

Synthesis of Chiral Tertiary Boronic Esters: Phosphonate-Directed Catalytic Asymmetric Hydroboration of Trisubstituted Alkenes.

Suman Chakrabarty, James M Takacs

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 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.

Suman ChakrabartyDepartment of Chemistry, University of Nebraska-Lincoln , Lincoln, Nebraska 68588-0304, United States.ORCID 0000-0002-6611-3839
James M TakacsDepartment of Chemistry, University of Nebraska-Lincoln , Lincoln, Nebraska 68588-0304, United States.ORCID 0000-0002-1903-6535

Funding

Catalytic Asymmetric Hydroboration: Uncapping the Potential with Two-Point Binding SubstratesR01GM100101 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI TAKACS, JAMES M · 2012 to 2020
$2.1M
NIGMS NIH HHS R01 GM100101
6 · The paper itself

Abstract

Highly enantioselective rhodium-catalyzed hydroboration of allylic phosphonates by pinacolborane affords chiral tertiary boronic esters. The β-borylated phosphonates are readily converted to chiral β- and γ-hydroxyphosphonates and aminophosphonates and to phosphonates bearing a quaternary carbon stereocenter. The utility of the latter is illustrated by the synthesis of (S)-(+)-bakuchiol methyl ether.

Indexed as

AlkenesBoronic AcidsCatalysisEstersMethyl EthersMolecular StructureOrganophosphonatesPhenolsRhodiumAlkenesbakuchiolBoronic AcidsEstersMethyl EthersOrganophosphonatesPhenolsRhodium

Identifiers

PMID28414243
PMCPMC5423446

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.