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Green Chemistry Letters and Reviews
United Kingdom · Taylor and Francis Ltd.
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Green Chemistry Letters and Reviews

Green Chemistry Letters and Reviews is a journal indexed in SJR in Environmental Chemistry and Chemistry (miscellaneous) with an H index of 58. It is an CC BY-NC Journal with a Single blind Peer Review review system, and It has a price of 540 €. The scope of the journal is focused on green chemistry, hazardous materials, environmental science. It has an SJR impact factor of 0,903 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,903.

ISSN: 1751-8253
Publisher: Taylor and Francis Ltd.
Category: Environmental Chemistry
Indexation: verifiedScopus / SJR verifiedWeb of Science verifiedDOAJ
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schedule CountryOfPapers database fields
SJR Impact Factor trending_up
0,903 Q1
H-index 58
Acceptance rate pie_chart
32%
Source Acceptance_Rate
Time to publication hourglass_top
34 weeks
Field Average_time_publication_weeks
Publication cost (APC) payments
540 € Open Access
Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science DOAJ

SJR Impact

0,903

H-index

58

Docs (year)

80

Docs 3y

184

Total refs

6415

Cites 3y

1087

Citable 3y

92

Cites/Doc 2y

5.62

Ref/Doc

80.19

Immediate OA

540 €

Embargoed OA

NPD

Non OA / Submission

- €

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Best articles by citations

An eco-friendly oxidative bromination of alkanones by an aqueous grinding technique

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ZnO-beta zeolite: as an effective and reusable heterogeneous catalyst for the one-pot synthesis of polyhydroquinolines

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Cesium carbonate catalyzed efficient synthesis of quinazoline-2,4(1H,3H)-diones using carbon dioxide and 2-aminobenzonitriles

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Cellulose sulfuric acid: reusable catalyst for solvent-free synthesis of bis(indolyl)methanes at room temperature

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Boric acid/glycerol as an efficient catalyst for regioselective epoxide ring opening by aromatic amines in water

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Bakers' yeast: an environment benign catalyst for the one-pot synthesis of indolyl chromenes and bisindolyl alkanes

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Aqueous ethanol: a suitable medium for the diastereoselective Diels-Alder reaction mediated by chiral bases

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An efficient synthesis of hemiaminal of indoles by using tetrabutylammonium fluoride (TBAF) in water as a reusable reaction media

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An efficient synthesis of a-hydroxyphosphonates and a-aminophosphonates in the presence of chlorotrimethylsilane

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An efficient synthesis of 3-benzylquinazolin-4(1H)-one derivatives under catalyst-free and solvent-free conditions

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An efficient one-pot synthesis of anthraquinone derivatives catalyzed by alum in aqueous media

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An efficient green protocol for the synthesis of chalcones by a Claisen-Schmidt reaction using bismuth(III)chloride as a catalyst under solvent-free condition

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An efficient and green one-pot three-component synthesis of 4,4'-(arylmethylene)bis(1H-pyrazol-5-ol)s catalyzed by 2-hydroxy ethylammonium propionate

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"Green Star": a holistic Green Chemistry metric for evaluation of teaching laboratory experiments

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A simple way of recycling of homogeneous catalyst in Suzuki reaction

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A new one pot and solvent-free synthesis of nickel porphyrin complex

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A mild, simple, and efficient approach to the synthesis of some novel 7-benzylidene-2,3-diphenyl-3,3a,4,5,6,7-hexahydro-2H-indazole derivatives

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A green synthesis of thieno[2,3-c]xanthen-6-ones through the tandem photochemical sigmatropic shift and cyclization

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A green and convenient approach for the synthesis of 1,10-phenanthrolines via a catalyst- and solvent-free condition

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A facile and efficient synthesis of tri- and tetrasubstituted imidazoles with potassium hydrogen sulfate and DB18C6 in an aqueous medium

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