ISSN: 0957-4166

Journal Home

Journal Guideline

Tetrahedron Asymmetry Q3 Unclaimed

Elsevier Ltd. United Kingdom

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

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, chiral, resolution, reduction, carbon, enzymatic, practical, bakers, absolute, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Catalysis (Q3) Inorganic Chemistry (Q3) Organic Chemistry (Q3) Physical and Theoretical Chemistry (Q3)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,396

SJR Impact factor

107

H Index

0

Total Docs (Last Year)

189

Total Docs (3 years)

0

Total Refs

290

Total Cites (3 years)

187

Citable Docs (3 years)

0

Cites/Doc (2 years)

0

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

Bioscience, Biotechnology and Biochemistry Q3
Rapid Communications in Mass Spectrometry Q3
Journal of Peptide Science Q3
Current Organic Chemistry Q3
Lipids Q3

Compare this journals

Aims and Scope

Best articles by citations

Practical synthesis of (3S,4S)-3-methoxy-4-methylaminopyrrolidine

Saponaceolides: Differential cytotoxicity and enantioselective synthesis of the right-hand lactone moiety

Congeners of Troeger's base as chiral ligands

Enzymatic Resolution of a-acetoxysulfides: A new approach to the synthesis of homochiral S,O-Acetals

Preparative resolution of 2-methyl-4-hexynic acid for the synthesis of optically active m-phenylene PGI2 derivatives and determination of their absolute configuration

A practical route to 3,6-dideoxyhexoses

Efficient resolution of naproxen by inclusion crystallization with N-octyl-glucamine and structure characterization of the inclusion complex

A simple preparative method for optically active glycidic esters

Enzymatic synthesis of (S)-(-)-1-(2-thienyl)propyl acetate

A polymer-bound oxazaborolidine catalyst: Enantioselective borane reductions of ketones

New fluorinated O-aryl lactic acids: Use as chiral derivatizing agents (CDAs) and determination of their enantiomeric purity with achiral diols

Study of asymmetric reduction of 1-substituted fluorenone with borane in the presence of several chiral amino alcohols

SHOW MORE ARTICLES

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

Asymmetric construction of benzylic quaternary carbons from chiral malonates: Formal synthesis of natural (-)aphanorphine

A convenient asymmetric synthesis of thalidomide

Design and synthesis of a chiral hapten for a radioimmunoassay of the antidepressant (2S, 3S, 5R)-2-(3,5-difluorophenyl)-3,5-dimethyl-2-morpholinol hydrochloride

Enantiomer resolution by crystallization with chiral hosts: application to monoterpenes, verbenone and apoverbenone

Enantiomer separation and absolute configuration of densely functionalized 2-oxatricyclo[4.3.1.03,8]decanes by CD spectroscopy and chemical correlation

Preparation of S-2-Ethylhexyl-para-methoxycinnamate by lipase catalyzed sequential kinetic resolution

Enantiomeric 2-anilino-2-oxo-1,3,2-oxazaphosphorinanes: Synthesis and NMR-investigation of their non-racemic mixtures

Radical reactions on furanoside acetals: A formal synthesis of (-)-canadensolide from D-mannose

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

Indoles from 3-nitropyridinium salts: A new route to chiral indoles and indolines

Synthesis of adenophostin A