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 €

Gold OA

-

Green 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

1-methyl-1H-2-pyrrolethiol and -selenol. Synthesis, tautomerism and autotransformations

2-Bromocyclohexanone Perhydrate - X-ray Crystal Structure and Conformational Effects on Reactivity in Sulfoxidations

2,2-Dichlorination of Aldehydes with the 2,6-Lutidine¬?HCl/Cl2/CH2Cl2 System: an Environmentally Benign Process Suitable for Scale Up

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

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

A Novel Thiolate Mediated Cyclization to OPC-15161

A Simple Synthesis of Morphine-3,6-di-beta-d-glucuronide

A Statistical Study of Density and Packing Variations among Crystalline Isomers

A Sulfoxide Version of the Julia-Lythgoe Olefination: A New Method for the Synthesis of Olefins from Carbonyl Compounds and Sulfoxides with Carbon-Carbon Coupling

A Synthetic Route to a New Surface-Active Phosphine Ligand: 12-DPDP (12-Diphenylphosphinododecylphosphonate)

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

Acid catalyzed rearrangement and acyl migration studies on 9-dihydro-13-acetylbaccatin-III, a major taxane from Taxus canadensis

SHOW MORE ARTICLES

An Efficient Synthesis of 11beta-(4-Aminophenyl)spiro[estr-4-ene-17beta,2'(5'H)-furan]-3,5'-dione

An Investigation of the Solid-State Photochemistry of a-Mesitylacetophenone Derivatives: Asymmetric Induction Studies and Crystal Structure-Reactivity Relationships

Aryl radical cyclisation onto pyrroles

Asymmetric Induction in Cobaloxime Complex Crystals Due to Chiral Crystal Environment

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

beta, gamma-Unsaturated a-amino ester derivatives by amination of gamma-silylated a,beta-unsaturated esters

Chemical Semisynthesis and Biotransformation with Rhizopus nigricans of Several Sesquiterpenes: Obtention of New 1a- and 2a-Hydroxyselinane Derivatives

Comparative Structural Characterization of the Biquaternized N-CH3 and N-BH3 Derivatives of the cis-Cyclen and cis-Cyclam Condensation Products with Glyoxal

Compelled Orientational Control of the Solid-State Photodimerization of trans -Cinnamamides: Dicarboxylic Acid as a Non-covalent Linker

Conformational control in the synthesis of mixed tetraethers of calix[4]arene. Part 2

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

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

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