ISSN: 0040-4020

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Tetrahedron Q2 Unclaimed

Elsevier Ltd. United Kingdom

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Tetrahedron is a journal indexed in SJR in Biochemistry and Drug Discovery with an H index of 221. It has a price of 2205 €. It has an SJR impact factor of 0,581 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,581.

Tetrahedron focuses its scope in these topics and keywords: synthesis, preparation, derivatives, synthetic, reactions, study, reaction, asymmetric, chiral, part, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Drug Discovery (Q2) Organic Chemistry (Q2) Biochemistry (Q3)

Price

2205 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,581

SJR Impact factor

221

H Index

465

Total Docs (Last Year)

2362

Total Docs (3 years)

26230

Total Refs

5335

Total Cites (3 years)

2349

Citable Docs (3 years)

2,31

Cites/Doc (2 years)

56,41

Ref/Doc

Other journals with similar parameters

International Journal of Biochemistry and Cell Biology Q2
Experimental Gerontology Q2
Advances in Neurobiology Q2
Current Chemical Genomics and Translational Medicine Q2
Biomolecules Q2

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Aims and Scope

Best articles by citations

Konbu'acidin A, a new bromopyrrole alkaloid with cdk4 inhibitory activity from Hymeniacidon sponge

Fluorescence Signalling of Transition Metal Ions by Multi-Component Systems Comprising 4-Chloro-1,8-naphthalimide as Fluorophore

Acetobromomaltose, a New Source of Carbohydrate Radicals. EPR Characterisation of Maltosyl and 2-Deoxymaltos-2-yl Radicals and Syntheses of Tetrasaccharide-like Mimics, Maltal, 3-a-Maltosyl Propiononitrile, 1,5-Anhydromaltitol and 2-Deoxymaltopyranos

Engineering Reactions in Crystalline Solids: Prediction of Intramolecular Carbene Rearrangements

Molecular amplification in a dynamic system by ammonium cations

A Facile Silyl Linker Strategy for the Solid-Phase Synthesis of Protected Glycopeptide: Synthesis of an N-Terminal Fragment of IL-2 (1-10)

Fast Galloylation of a Sugar Moiety: Preparation of Three Monogalloylsucroses as References for Antioxidant Activity. A Method for the Selective Deprotection of tert-Butyldiphenylsilyl Ethers

Synthesis of desymmetrized, enantiopure dihydro-methano-diarylazocines: topologically interesting eyeteaser molecules

The development of strategies for construction of the aziridine core of the antitumor agents azinomycins A and B

TiCl4-Mediated Nucleophilic Substitution of Propargylic Esters

Solid State Photochemistry of Isocoumarins and Isothiocoumarins

A Convenient Method for Synthesis of Optically Active Methylphenidate from N-Methoxycarbonylpiperidine by Utilizing Electrochemical Oxidation and Evans Aldol-type Reaction

SHOW MORE ARTICLES

The Synthesis of 1,(7)-Substituted Pyrrolizidin-3-ones

Energy Transfer Studied Using Spin Polarized Free Radicals. Effect of Substrate Structure and a Comparison Between Micellar Confinement and Free Solution

Synthesis of abeta-Unsaturated Trifluoromethyl Ketones from 4-Dimethylamino-1,1,1-trifluorobut-3-ene-2-one by Addition of Grignard Reagents

Nickel Catalyzed Hydrovinylation of Arylethylenes: General Method of Synthesis of a-Arylpropionic Acids Intermediates

Nitration of N-acetyl enamines with acetyl nitrate

Construction of Peptides That Undergo Structural Transition from a-Helix to beta-Sheet and Amyloid Fibril Formation by the Introduction of N-Terminal Hydrophobic Amino Acids

Reactions of (Aryl)(chloro)methyl p-Tolyl Sulfoxides with Tetrasulfur Tetranitride (S4N4): Formation and Characterization of 3,5-Diaryl-1,2,4,6-thiatriazine 1-Oxides

Regio- and diastereoselective dialkylation of (4S)-2,4-dimethyl-2,4-dihydro-1H-pirazino[2,1-b]quinazoline-3,6-dione

Shape and Size Effects in the Crystal Structures of Complexes of 1,3,5-Trinitrobenzene with some Trigonal Donors: The Benzene-Thiophene Exchange Rule

Controlling the Size of Vesicles Prepared from Egg Lecithin using a Hydrotrope

Reactions of alkylidenephosphoranes with symmetrically substituted p-quinones

Azoles. Part 43: Reactions of N-(Phenylsulphonylmethyl)- and N-(Phenylsulphinylmethyl)azoles with some Nitroarenes

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