TETRAHEDRON LETTERS

TETRAHEDRON LETTERS

TETRAHEDRON LETT
影响因子:1.5
是否综述期刊:
是否预警:不在预警名单内
是否OA:
出版国家/地区:ENGLAND
出版社:Elsevier Ltd
发刊时间:1959
发刊频率:Weekly
收录数据库:SCIE/Scopus收录
ISSN:0040-4039

期刊介绍

Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
《四面体快报》最大限度地传播了有机化学的杰出发展。该杂志每周出版一次,内容包括实验和理论有机化学中的技术、结构、方法和结论的发展。及时而重要的研究成果的快速发表使世界各地的研究人员能够将他们的新贡献迅速传播给大量的国际受众。
年发文量 358
国人发稿量 157.27
国人发文占比 0.44%
自引率 -
平均录取率0
平均审稿周期 平均1.3个月平均4.8周
版面费 US$3690
偏重研究方向 化学-有机化学
期刊官网 http://www.sciencedirect.com/science/journal/00404039
投稿链接 https://www.editorialmanager.com/TETL

期刊高被引文献

Nondissociative chain walking as a strategy in catalytic organic synthesis
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.07.029
Alkylation reactions of benzothiazoles with N,N-dimethylamides catalyzed by the two-component system under visible light
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.064
Alstobrogaline, an unusual pentacyclic monoterpenoid indole alkaloid with aldimine and aldimine-N-oxide moieties from Alstonia scholaris
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.02.018
Ultraviolet irradiation of terarylenes: A facile, efficient, and environmentally friendly method for the synthesis of fused polycyclic products
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.063
Eosin Y catalysed visible-light mediated aerobic oxidation of tertiary amines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151041
A new strategy for utilizing activated CH-group to construct a FRET platform for ratiometric sensing of cyanides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.010
Ca(II)-catalyzed diastereoselective formal [4+2] annulation of a 3-component solvent-free povarov reaction
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.021
α-Amidoboronate esters by amide-directed alkane C H borylation
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.020
An efficient synthesis of 2-isoxazolines from α-haloketone oximes and dimethyl sulfonium salts
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.062
Chiral Brønsted acid-catalyzed Friedel–Crafts reaction of 3-indolylsulfamidates with indoles: Synthesis of enantioenriched bisindolylmethane sulfamates
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.003
Colorimetric and ratiometric sensors derivated from natural building blocks for fluoride ion detection
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151330
PhI(OAc)2-mediated alkoxyoxygenation of β,γ-unsaturated ketoximes: Preparation of isoxazolines bearing two contiguous tetrasubstituted carbons
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.046
Heterogeneous gold-catalyzed oxidative cross-coupling of propargylic acetates with arylboronic acids leading to (E)-α-arylenones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.11.053
[4 + 3]-Cycloaddition of aza-o-quinone methides and azomethine imines to make 1,2,4-triazepines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.038
First Cp*Co(III)-Catalyzed Mizoroki-Heck Coupling Reactions of Alkenes and Aryl bromide/Iodide
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151283
Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151080
Copper-catalyzed enantioselective addition of alcohols to isatin-derived ketimines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.049
Thalicfoetine, a novel isoquinoline alkaloid with antibacterial activity from Thalictrum foetidum
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151135
Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.04.014
First synthesis and further derivatization of furo[3,2-c]pyrazol-6-ones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.01.021
Simple one pot synthesis of ketone from carboxylic acid using DCC as an activator
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.04.030
Unexpected intramolecular nucleophilic cyclization of ureidoacetamide: A novel route towards the synthesis of 2,4,5-trisubsituted oxazoles
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.028
Iron-catalyzed δ-selective conjugate addition of methyl and cyclopropyl Grignard reagents to α,β,γ,δ-unsaturated esters and amides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.043
Investigation of α-amino acid N-carboxyanhydrides by X-ray diffraction for controlled ring-opening polymerization
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.028
Three-component couplings for the synthesis of pyrroloquinoxalinones by azomethine ylide 1,3-dipolar cycloaddition chemistry
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151023
Enantioselective synthesis of chiral carbocyclic pyrimidine nucleosides via asymmetric cyclopropanation
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151183
Epoxide as precatalyst for metal-free catalytic transesterification
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.056
Violet/deep-blue fluorescent organic light-emitting diode based on high-efficiency novel carbazole derivative with large torsion angle
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151340
Total synthesis of the tricyclic humulanolide wilfolide B
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.058
I2/TBHP mediated multiple C H bonds functionalization of azaarenes with methylarenes to synthesize iodoisoquinolinones via iodination/N-benzylation/amidation sequence
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151328
Propargyl α-aryl-α-diazoacetates as robust reagents for the effective C-H bond functionalization of 1,3-diketones via scandium catalysis
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.026
First total synthesis of versicotide D and analogs
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151281
Triphenylene based metal-pyridine cages
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151202
Facile and practical synthesis of π-extended oxepins by benzannulation and intramolecular cyclization
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.008
Type-II Pauson-Khand reaction of 1,8-enyne in the attempt of building 7/5 ring of (-)-caribenol A and DFT understanding
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151001
Functionalization of silica gel by ultrasound-assisted surface Suzuki coupling
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.07.028
The DFT study on Rh–C bond dissociation enthalpies of (iminoacyl)rhodium(III)hydride and (iminoacyl)rhodium(III)alkyl
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.042
Xanthate-mediated synthesis of functional bis(γ-thiolactones)
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.004
First asymmetric enantioselective total synthesis of phenanthridine alkaloid, (S)-(+)-asiaticumine and its enantiomer
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151278
Total synthesis and determination of the absolute configuration of paralemnolin C and biological studies of eremophilane derivatives
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.026
Triptycene-scaffolded tetraphenylethylenes with irregular temperature-dependence AIE
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.069
Synergic effect of hydrogen bonding and dipole repulsion in the ring-closing metathesis of N-homoallyl-2-(hydroxymethyl)acrylamides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.011
Room Temperature Pd(0)/Ad3P-Catalyzed Coupling Reactions of Aryl Chlorides with Bis(pinacolato)diboron
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.01.042
Diphosphination of ortho-quinone methide precursors with diphosphines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.055
Photoaddition reactions of azomethine ylides generated from α-aminonitriles to fullerene C60: Formation of fulleropyrrolidines and reaction efficiencies changes depending on reaction conditions
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151208
Transfer hydrogenation of ketones catalyzed by 2,6‐bis(triazinyl)pyridine ruthenium complexes: The influence of alkyl arms
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.150993
Studies towards the stereoselective total synthesis of Gliomasolide A
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151169
One-pot synthesis of new iso-DPP derivatives from terminal alkynes and isocyanates
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151079
Stereoconvergent synthesis of N-Boc-(2R,3S)-3-hydroxy-2-phenylpiperidine
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.02.005
Alkaloids of NIRAM, natural dye from Polygonum tinctorium, and their anti-inflammatory activities
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151130

质量指标占比

研究类文章占比 OA被引用占比 撤稿占比 出版后修正文章占比
99.72%4.31%-0.89%

相关指数

影响因子
影响因子
年发文量
自引率
Cite Score

预警情况

查看说明
时间 预警情况
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
*来源:中科院《 国际期刊预警名单》

JCR分区

WOS分区等级:Q3区
版本 按学科 分区
WOS期刊SCI分区
WOS期刊SCI分区
WOS期刊SCI分区是指SCI官方(Web of Science)为每个学科内的期刊按照IF数值排 序,将期刊按照四等分的方法划分的Q1-Q4等级,Q1代表质量最高,即常说的1区期刊。
(2024-2025年最新版)
CHEMISTRY, ORGANIC
Q3

中科院分区

查看说明
版本 大类学科 小类学科 Top期刊 综述期刊
2025年3月最新升级版
化学4区
CHEMISTRY, ORGANIC 有机化学
4区
2023年12月升级版
化学4区
CHEMISTRY, ORGANIC 有机化学
4区
2022年12月旧的升级版
化学4区
CHEMISTRY, ORGANIC 有机化学
4区