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Journal of Sulfur Chemistry
United Kingdom · Taylor and Francis Ltd.
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Journal of Sulfur Chemistry

Journal of Sulfur Chemistry is a journal indexed in SJR in Chemistry (miscellaneous) with an H index of 40. It has a price of 2395 €. It has an SJR impact factor of 0,309 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,309.

ISSN: 1741-5993
Publisher: Taylor and Francis Ltd.
Category: Chemistry (miscellaneous)
Indexation: verifiedScopus / SJR verifiedWeb of Science
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schedule CountryOfPapers database fields
SJR Impact Factor trending_up
0,309 Q3
H-index 40
Acceptance rate pie_chart
34%
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
2.395 € Subscription
Non-OA path 0 €

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

SJR Impact

0,309

H-index

40

Docs (year)

58

Docs 3y

154

Total refs

2671

Cites 3y

319

Citable 3y

154

Cites/Doc 2y

1.92

Ref/Doc

46.05

Immediate OA

2395 €

Embargoed OA

NPD

Non OA / Submission

0 €

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Best articles by citations

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ZrCl4/NaI and ZrOCl2 ¬? 8H2O/NaI as effective systems for reductive coupling of sulfonyl chlorides and chemoselective deoxygenation of sulfoxides

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Determination of the promoting effect of nano SiO2and H3PO4@nano SiO2in the thiocyanation ofN-containing aromatic compounds under solvent-free conditions

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Copper(I) selenophene-2-carboxylate (CuSC) promoted C-S cross-coupling reaction of thiols with aryl iodides

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Convenient syntheses of N-methylthioamides: A migration of the H2S molecule in the thioamide-nitrile system

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Comparison of the reactivities of 2-mercaptoaniline and 2-hydroxyaniline with 2-chloronicotinoyl chloride

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Chemoselective synthesis of phosphorus ylides through the reaction of 2-mercaptobenzimidazole and 2-hydroxybenzimidazole with triphenylphosphine and acetylenic esters

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Capture of solar energy using elemental sulfur

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beta-Aminocrotononitrile in heterocyclic synthesis: Synthesis of polysubstituted pyridines as precursors to bicycles and polycycles

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An efficient, basic resin mediated, one-pot synthesis of O-alkyl-S-methyl dithiocarbonates from the corresponding alcohols

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An efficient, basic resin mediated, one-pot synthesis of dithiocarbazates from the corresponding alkyl halides

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An efficient, basic resin mediated, one-pot synthesis of dithiocarbamate esters through alcoholic tosylates

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