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verified SJR 1,928 · Q1 • database Scopus / SJR & Web of Science indexed
Green Chemistry
United Kingdom · Royal Society of Chemistry
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Green Chemistry

Green Chemistry is a journal indexed in SJR in Pollution and Environmental Chemistry with an H index of 288. It has an SJR impact factor of 1,928 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,928.

Green Chemistry focuses its scope in these topics and keywords: ionic, catalyst, production, catalysis, renewable, reactions, oxidation, catalysts, epoxy, biomassderived, ...

ISSN: 1463-9262
Publisher: Royal Society of Chemistry
Category: Pollution
Indexation: verifiedScopus / SJR verifiedWeb of Science
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schedule CountryOfPapers database fields
SJR Impact Factor trending_up
1,928 Q1
H-index 288
Acceptance rate pie_chart
18% Selective
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
NPD Open Access
Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

SJR Impact

1,928

H-index

288

Docs (year)

875

Docs 3y

2623

Total refs

67801

Cites 3y

25957

Citable 3y

2613

Cites/Doc 2y

9.15

Ref/Doc

77.49

Immediate OA

—

Embargoed OA

0 €

Non OA / Submission

—

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Best articles by citations

Base catalysts immobilised on silica coated reactor walls for use in continuous flow systems

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Water promoted organic chemistry

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Ene reaction of allylbenzene and N-methylmaleimide in subcritical water and ethanol

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Efficient solvent-free O-silylation of alcohols with R3SiCl

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Dechlorination of pentachlorophenol in supercritical carbon dioxide with a zero-valent silver-iron bimetallic mixture

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Convenient and rapid microwave-assisted synthesis of pyrido-fused ring systems applying the tert-amino effect

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Construction of the di(trimethylolpropane) cross linkage and the phenylnaphthalene structure coupled with selective beta-O-4 bond cleavage for synthesizing lignin-based epoxy resins with a controlled glass transition temperature

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Conjugate additions of heteronucleophiles to enones and alkynoates. A 'benign by design' functionalization of heteroaromatics

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Combined microwave and ultrasound accelerated Knoevenagel-Doebner reaction in aqueous media: a green route to 3-aryl acrylic acids

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Clean and efficient syntheses of calix[4]arene modified polymer supports

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Bioconversion of toluene to p-hydroxybenzoate

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"Green" oxidation reactions - application to carbohydrate chemistry

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Asymmetric epoxidation of olefins

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Aqueous N-alkylation of amines using alkyl halides: direct generation of tertiary amines under microwave irradiation

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An expeditious synthesis of 1-aryl-4-methyl-1,2,4-triazolo[4,3-a]quinoxalines under solvent-free conditions using iodobenzene diacetate

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