ISSN: 0899-0042

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Chirality Q3 Unclaimed

Wiley-Liss Inc. United States

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Chirality is a journal indexed in SJR in Drug Discovery and Pharmacology with an H index of 81. It has a price of 2500 €. It has an SJR impact factor of 0,382 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,382.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Analytical Chemistry (Q3) Catalysis (Q3) Drug Discovery (Q3) Organic Chemistry (Q3) Pharmacology (Q3) Spectroscopy (Q3)

Price

2500 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,382

SJR Impact factor

81

H Index

119

Total Docs (Last Year)

303

Total Docs (3 years)

6056

Total Refs

615

Total Cites (3 years)

301

Citable Docs (3 years)

2.1

Cites/Doc (2 years)

50.89

Ref/Doc

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Aims and Scope

Best articles by citations

Steric aspects of formoterol and terbutaline: Is there an adverse effect of the distomer on airway smooth muscle function?

Preparative resolution of 1-aminoindan-1,5-dicarboxylic acid (AIDA) by chiral ligand-exchange chromatography

Book Review

Convenient lipase-assisted preparation of both enantiomers of suprofen, a non-steroidal anti-inflammatory drug

Chiral aldehydes in hydrocarbons: diastereoselective nucleophilic addition, NMR, and CD spectroscopy reveal dynamic solvation effects

Chiral aminophosphonate eluent for enantiomeric analysis of amino acids

Secondary phosphine oxides: tautomerism and chiral recognition monitored by multinuclear NMR spectroscopy of their Rh2[(R)-MTPA]4 adducts

Chiral analysis of butaclamol enantiomers in human plasma by HPLC using a macrocyclic antibiotic (vancomycin) chiral stationary phase and solid phase extraction

Enantiofacial selective reduction of 2-allyl-2-carboethoxy-cyclopentanone mediated by baker's yeast

Trans-diaryl epoxides: Asymmetric synthesis, ring-opening, and absolute configuration

Chiral derivatives of 2-(1-naphthyl)-2-phenylacetic acid

Chiral discrimination by HPLC on aryl carbamate derivatives of chitin coated onto microporous aminopropyl silica

SHOW MORE ARTICLES

Differential recognition of resveratrol isomers by the human estrogen receptor-?: Molecular dynamics evidence for stereoselective ligand binding

Determination of the enantiomeric composition of mexiletine and its four hydroxylated metabolites in urine by enantioselective capillary gas chromatography

Enantiomeric resolution of kielcorin derivatives by HPLC on polysaccharide stationary phases using multimodal elution

Chiral effect on a self-assembling bicopper complex

Use of a naphthylethylcarbamoylated-?-cyclodextrin chiral stationary phase for the separation of drug enantiomers and related compounds by sub- and supercritical fluid chromatography

Enantiomeric separation of dansyl amino acids using macrocyclic antibiotics as chiral mobile phase additives by narrow-bore high-performance liquid chromatography

Comparison of the chiral separation of amino-acid derivatives by a teicoplanin andRN-?-CD CSPs using waterless mobile phases: Factors that enhance resolution

Enantioresolution of fluorinated diphenylmethanols and determination of their absolute configurations by X-Ray crystallographic and1H NMR anisotropy methods

Assignment of absolute configuration of chiral carboxylic acids via exciton-coupled CD treatment: 4-phenylthioproline as a case study

Myocardial uptake of thiopental enantiomers by the isolated perfused rat heart

Enantioselective chromatography and molecular modeling of novel aryloxyaminopropan-2-ols with the alkyl carbamate function

Utilizing hydrolases of opposite enantiopreference for the preparation of both enantiomers of (1R,7aR)-(?)- and (1S,7aS)-(+)-3,6,7,7a-tetrahydro-1-hydroxy-7a-methyl-1H-inden-5(2H)-one