About the journal
Tetrahedron Chem is an open-access journal published by Elsevier in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared review time at DOAJ: 9 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier
- ISSN
- 2666-951X
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Articles in DOAJ
- 156
- Declared review time
- 9 weeks
- Declared peer-review model
- other
- Official website
- https://www.sciencedirect.com/journal/tetrahedron-chem
Index listings
- DOAJ · 2022-04-11
- Indexing
- DOAJ
- APC
- —
- Declared review time (DOAJ)
- 9 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
Methodology signals (dated facts from their sources)
Details of the evaluation under the published methodology are shown to signed-in users (free).
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
156
Most recent article
last month
Average review time (journal-declared via DOAJ)
9weeks
Works in OpenAlex
153
Last recorded publication year
2026
h-index
15
i10-index
33
From OpenAlex open data (CC0).
Editorial & policy10
- Last DOAJ review date
- 2026-04-27
- Added to DOAJ
- 2022-04-11
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 93%
- ORCID iDs in current deposits
- 86%
- Deposits licence metadata at Crossref
- ✓
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9918382989006676
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Catalytic C–H Functionalization Methods
- Catalytic C–H Functionalization Methods
- Asymmetric Synthesis and Catalysis
- Radical Photochemical Reactions
- Catalytic C–H Functionalization Methods
- Radical Photochemical Reactions
- Catalytic Cross-Coupling Reactions
- Radical Photochemical Reactions
Show all subjects (75)
- Asymmetric Hydrogenation and Catalysis
- Asymmetric Hydrogenation and Catalysis
- Catalytic Alkyne Reactions
- Fluorine in Organic Chemistry
- Asymmetric Synthesis and Catalysis
- Asymmetric Synthesis and Catalysis
- Fluorine in Organic Chemistry
- Organic Chemistry Synthesis Methods
- Catalytic Cross-Coupling Reactions
- Sulfur-Based Synthesis Techniques
- Sulfur-Based Synthesis Techniques
- Catalytic Cross-Coupling Reactions
- Sulfur-Based Synthesis Techniques
- Catalytic Alkyne Reactions
- Synthesis and Catalytic Reactions
- Cyclopropane Reaction Mechanisms
- Catalytic Alkyne Reactions
- Cyclopropane Reaction Mechanisms
- Cyclopropane Reaction Mechanisms
- Advanced Synthetic Organic Chemistry
- Asymmetric Hydrogenation and Catalysis
- Fluorine in Organic Chemistry
- Synthesis and Catalytic Reactions
- Chemical Synthesis and Analysis
- Chemical Synthesis and Analysis
- Oxidative Organic Chemistry Reactions
- Oxidative Organic Chemistry Reactions
- Oxidative Organic Chemistry Reactions
- Axial and Atropisomeric Chirality Synthesis
- Click Chemistry and Applications
- Click Chemistry and Applications
- Carbon dioxide utilization in catalysis
- Chemical Synthesis and Analysis
- Carbon dioxide utilization in catalysis
- Click Chemistry and Applications
- N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
- Synthetic Organic Chemistry Methods
- Organoboron and organosilicon chemistry
- Microbial Natural Products and Biosynthesis
- Synthetic Organic Chemistry Methods
- Microbial Natural Products and Biosynthesis
- Chemical Synthesis and Reactions
- Enzyme Catalysis and Immobilization
- Chemical Reactions and Mechanisms
- Chemical Reaction Mechanisms
- Organoboron and organosilicon chemistry
- Organometallic Complex Synthesis and Catalysis
- Chemical Synthesis and Reactions
- Organoboron and organosilicon chemistry
- Chemical synthesis and alkaloids
- Molecular spectroscopy and chirality
- Synthesis and Biological Evaluation
- Synthesis of Indole Derivatives
- Organic Chemistry Cycloaddition Reactions
- Supramolecular Chemistry and Complexes
- Molecular spectroscopy and chirality
- Synthesis and Biological Evaluation
- Chemical synthesis and alkaloids
- Luminescence and Fluorescent Materials
- Synthesis and Properties of Aromatic Compounds
- Axial and Atropisomeric Chirality Synthesis
- Marine Sponges and Natural Products
- Traditional and Medicinal Uses of Annonaceae
- Axial and Atropisomeric Chirality Synthesis
- Marine Sponges and Natural Products
- Traditional and Medicinal Uses of Annonaceae
- Luminescence and Fluorescent Materials
Keywords (DOAJ)
- organic chemistry
- organic materials
- catalysis
- synthetic methology
- sustainable synthesis
- stereochemistry
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ