verified SJR 0,426 · Q3 • database Scopus / SJR & Web of Science indexed

United Kingdom · Elsevier Ltd

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Tetrahedron

Tetrahedron is a journal indexed in SJR in Biochemistry and Drug Discovery with an H index of 241. It has a price of 2205 €. It has an SJR impact factor of 0,426 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,426.

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

ISSN: 0040-4020

Editorial: Elsevier Ltd

Category: Biochemistry

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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SJR Impact Factor trending_up

0,426 Q3

H-index 241

Tasa de Aceptación pie_chart

19% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

2.205 € Subscription

Ruta Non-OA 0 €

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,426

H-index

241

Docs (year)

426

Docs 3y

1295

Total refs

23380

Cites 3y

2931

Citable 3y

1291

Cites/Doc 2y

2.3

Ref/Doc

54.88

Immediate OA

2205 €

Embargoed OA

NPD

Non OA / Submission

0 €

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Best articles by citations

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

Water-Accelerated Aldol Reaction of Ketene Silyl Acetals with Carbonyl Compounds

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

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

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

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

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

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

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

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

Asymmetric Induction in Cobaloxime Complex Crystals Due to Chiral Crystal Environment

Aryl radical cyclisation onto pyrroles

SHOW MORE ARTICLES

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

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

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

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

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

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 Statistical Study of Density and Packing Variations among Crystalline Isomers

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

A Novel Thiolate Mediated Cyclization to OPC-15161

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

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

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