ISSN: 0899-0042

Journal Home

Journal Guideline

Chirality Q2 Unclaimed

Wiley-Liss Inc. United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Chirality is a journal indexed in SJR in Drug Discovery and Pharmacology with an H index of 83. It has a price of 2500 €. It has an SJR impact factor of 0,438 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,438.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Analytical Chemistry (Q2) Catalysis (Q3) Drug Discovery (Q3) Organic Chemistry (Q3) Pharmacology (Q3) Spectroscopy (Q3)

Price

2500 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,438

SJR Impact factor

83

H Index

87

Total Docs (Last Year)

326

Total Docs (3 years)

4801

Total Refs

782

Total Cites (3 years)

321

Citable Docs (3 years)

2.77

Cites/Doc (2 years)

55.18

Ref/Doc

Comments

No comments ... Be the first to comment!

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID *

* The email or ORCID field is only to validate the authenticity of the comment, the identity will not be public. .

Other journals with similar parameters

Biomolecules and Therapeutics Q2
PPAR Research Q2
Current Drug Targets Q2
Journal of Gene Medicine Q2
Current Gene Therapy Q2

Compare this journals

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