Tetrahedron Letters
Published by Elsevier
ISSN : 0040-4039 eISSN : 1873-3581
Abbreviation : Tetrahedron Lett.
Aims & Scope
Tetrahedron Letters provides rapid dissemination of short accounts of advances of outstanding significance and timeliness in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Communications in Tetrahedron Letters are expected to represent brief summaries of preliminary work or initial results at the cutting edge of the field.
Rapid publication of such research enables authors to transmit their new contributions quickly to a large, international audience.
Tetrahedron Letters also publishes 'Digests', commissioned short reviews, highlights or perspectives, focusing on recent advancements in a field.
View Aims & ScopeMetrics & Ranking
Impact Factor
| Year | Value |
|---|---|
| 2025 | 1.5 |
| 2024 | 1.50 |
SJR (SCImago Journal Rank)
| Year | Value |
|---|---|
| 2024 | 0.334 |
Quartile
| Year | Value |
|---|---|
| 2024 | Q3 |
h-index
| Year | Value |
|---|---|
| 2024 | 186 |
Journal Rank
| Year | Value |
|---|---|
| 2024 | 15605 |
Journal Citation Indicator
| Year | Value |
|---|---|
| 2024 | 2459 |
Impact Factor Trend
Abstracting & Indexing
Journal is indexed in leading academic databases, ensuring global visibility and accessibility of our peer-reviewed research.
Subjects & Keywords
Journal’s research areas, covering key disciplines and specialized sub-topics in Biochemistry, Genetics and Molecular Biology, Chemistry and Pharmacology, Toxicology and Pharmaceutics, designed to support cutting-edge academic discovery.
Most Cited Articles
The Most Cited Articles section features the journal's most impactful research, based on citation counts. These articles have been referenced frequently by other researchers, indicating their significant contribution to their respective fields.
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A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
Citation: 4857
Authors: Kenkichi, Yasuo, Nobue
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A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
Citation: 2003
Authors: Norio, Kinji, Akira
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Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Citation: 1702
Authors: S.L., M.H.
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Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds
Citation: 1634
Authors: E.J., J.William
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A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
Citation: 1508
Authors: E.J., P.L.
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The use of microwave ovens for rapid organic synthesis
Citation: 1426
Authors: Richard, Frank, Kenneth, Humera, Lorraine, Lena, John
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New N- and O-arylations with phenylboronic acids and cupric acetate
Citation: 1084
Authors: Dominic M.T, Kevin L, Ru-Ping, Michael P
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New aryl/heteroaryl Cî—¸N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
Citation: 996
Authors: Patrick Y.S, Charles G, Simon, Jessica, Michael P, Dominic M.T, Andrew