Evidence map›Paper›PMID 26196673›Full record

ArticleThe Journal of organic chemistry2015

Modular, Metal-Catalyzed Cycloisomerization Approach to Angularly Fused Polycyclic Aromatic Hydrocarbons and Their Oxidized Derivatives.

Paul F Thomson, Damon Parrish, Padmanava Pradhan, Mahesh K Lakshman

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2015. 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
2.4field-weighted citation impact, top 11% of its field
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, 24 citations in OpenAlex.

  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

4 authors at 2 institutions in 1 country.

Paul F Thomson†Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, New York 10031, United States.
Damon Parrish‡Naval Research Laboratory, Code 6030, 4555 Overlook Avenue, Washington D.C. 20375, United States.
Padmanava Pradhan†Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, New York 10031, United States.
Mahesh K Lakshman†Department of Chemistry, The City College and The City University of New York, 160 Convent Avenue, New York, New York 10031, United States.
City College of New York · USUnited States Naval Research Laboratory · US

Funding

VOLTAGE GATING OF ION CHANNELS--SIMULATIONS AND AB INITIO CALCULATIONSS06GM008168 · NIGMS · CITY COLLEGE OF NEW YORK · PI LAKSHMAN, MAHESH K · 1989 to 2010
$17.6M
Cellular/Molecular Basis of Development: Research CenterG12MD007603 · NIMHD · CITY COLLEGE OF NEW YORK · PI PEZZANO, MARK · 2012 to 2017
$11.5M
Studies in Chemical CarcinogenesisF31GM082025 · NIGMS · CITY COLLEGE OF NEW YORK · PI THOMSON, PAUL FERNANDO · 2008 to 2009
$52k
NIGMS NIH HHS F31 GM082025NIGMS NIH HHS S06 GM008168NIMHD NIH HHS G12 MD007603NIMHD NIH HHS G12MD007603
6 · The paper itself

Abstract

Palladium-catalyzed cross-coupling reactions of 2-bromobenzaldehyde and 6-bromo-2,3-dimethoxybenzaldehyde with 4-methyl-1-naphthaleneboronic acid and acenaphthene-5-boronic acid gave corresponding o-naphthyl benzaldehydes. Corey-Fuchs olefination followed by reaction with n-BuLi led to various 1-(2-ethynylphenyl)naphthalenes. Cycloisomerization of individual 1-(2-ethynylphenyl)naphthalenes to various benzo[c]phenanthrene (BcPh) analogues was accomplished smoothly with catalytic PtCl2 in PhMe. In the case of 4,5-dihydrobenzo[l]acephenanthrylene, oxidation with DDQ gave benzo[l]acephenanthrylene. The dimethoxy-substituted benzo[c]phenanthrenes were demethylated with BBr3 and oxidized to the o-quinones with PDC. Reduction of these quinones with NaBH4 in THF/EtOH in an oxygen atmosphere gave the respective dihydrodiols. Exposure of the dihydrodiols to N-bromoacetamide in THF-H2O led to bromohydrins that were cyclized with Amberlite IRA 400 HO(-) to yield the series 1 diol epoxides. Epoxidation of the dihydrodiols with mCPBA gave the isomeric series 2 diol epoxides. All of the hydrocarbons as well as the methoxy-substituted ones were crystallized and analyzed by X-ray crystallography, and these data are compared to other previously studied BcPh derivatives. The methodology described is highly modular and can be utilized for the synthesis of a wide variety of angularly fused polycyclic aromatic hydrocarbons and their putative metabolites and/or other derivatives.

Indexed as

BenzaldehydesBoronic AcidsCatalysisCrystallography, X-RayIsomerismNaphthalenesOxidation-ReductionPhenanthrenesPolycyclic Aromatic Hydrocarbons2-bromobenzaldehyde4-methyl-1-naphthaleneboronic acid6-bromo-2,3-dimethoxybenzaldehydeBenzaldehydesBoronic AcidsNaphthalenesPhenanthrenesPolycyclic Aromatic Hydrocarbons

Identifiers

PMID26196673
PMCPMC4541800
OpenAlexW2401622081

What OpenQuestion holds

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Read underepoch 390

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.