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verified SJR 0,396 · Q3
Tetrahedron Asymmetry
United Kingdom · Elsevier Ltd.
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Tetrahedron Asymmetry

Tetrahedron Asymmetry is a journal indexed in SJR in Organic Chemistry and Catalysis with an H index of 107. It has an SJR impact factor of 0,396 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,396.

Tetrahedron Asymmetry focuses its scope in these topics and keywords: synthesis, asymmetric, resolution, chiral, reduction, enzymatic, practical, carbon, building, citronellol, ...

ISSN: 0957-4166
Publisher: Elsevier Ltd.
Category: Organic Chemistry
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SJR Impact Factor trending_up
0,396 Q3
H-index 107
Acceptance rate pie_chart
24% Selective
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
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Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

SJR Impact

0,396

H-index

107

Docs (year)

0

Docs 3y

189

Total refs

0

Cites 3y

290

Citable 3y

187

Cites/Doc 2y

0

Ref/Doc

0.0

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Combined microbial oxidation and reduction: a new approach to the highyield synthesis of homochiral unsaturated secondary alcohols from racemates

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cis-2-amino-3,3-dimethyl-1-indanol: Synthesis, resolution, and application as a highly efficient chiral auxiliary

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Chiral ligands derived from Abrine. 1. Synthesis of sec- and tert-beta-amino alcohols and catalysis for enantioselective addition of diethylzinc toward aromatic aldehydes

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Chiral C2-symmetric 2,5-disubstituted pyrrolidine derivatives as chiral catalyst ligands in the reaction of diethylzinc with arylaldehydes

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Chemoenzymatic synthesis of ferrulactone II and (2E)-9-hydroxydecenoic acid

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Catalytic asymmetric synthesis of a versatile intermediate for diterpene syntheses. Regioselective olefin insertion in asymmetric Heck reactions

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C2-Symmetric bisphosphinites and a bisaminophosphine as new chiral ligands for Pd-catalyzed asymmetric allylic substitution

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Asymmetric reduction of substituted fluorenones with aluminium lithium hydride in the presence of chiral amino alcohols

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