Default: Green Chemistry

ISSN: 1463-9262

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Green Chemistry Q1 Unclaimed

Royal Society of Chemistry United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Green Chemistry is a journal indexed in SJR in Pollution and Environmental Chemistry with an H index of 205. It has an SJR impact factor of 2,259 and it has a best quartile of Q1. It is published in English.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Price

- €

Gold OA

-

Green OA

- €

Non OA

Metrics

Green Chemistry

2,259

SJR Impact factor

205

H Index

658

Total Docs (Last Year)

1855

Total Docs (3 years)

42902

Total Refs

17949

Total Cites (3 years)

1822

Citable Docs (3 years)

9,81

Cites/Doc (2 years)

65,2

Ref/Doc


Best articles

"Green" oxidation reactions - application to carbohydrate chemistry

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A green chemistry approach to the synthesis of a crystalline organic inclusion compound

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A more benign approach to the synthesis of calixarenes

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A novel single step synthesis of 2-methyl-6-phenylpyridine from non-heterocyclic compounds over molecular sieve catalysts

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A practical improvement of odorless Corey-Kim and Swern oxidations

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Alkylation of dihydroxybenzenes and anisole with methyl-tert-butyl ether (MTBE) over solid acid catalysts

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An efficient magnetic carbon-based solid acid treatment for corncob saccharification with high selectivity for xylose and enhanced enzymatic digestibility

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

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Asymmetric epoxidation of olefins

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Atomically dispersed Ni as the active site towards selective hydrogenation of nitroarenes

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Award

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SHOW MORE ARTICLES

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

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Bioconversion of toluene to p-hydroxybenzoate

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

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

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

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

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Editorial

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Editorial

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Efficient solvent-free O-silylation of alcohols with R3SiCl

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

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