Impact Factor
4.08
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
3.50
12,662 total citations
h5-index
58
h5 depth signal
Cited share
86.5%
3,143 of 3,634
Total citations
12,662
Citation footprint
Metric signal
3.29
External metric anchor
Self-citation
12.3%
1,558 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
5,995
United States
2,479
India
1,999
Japan
1,301
Germany
707
Citing Fields of Research
Synthesis
15,502
Catalysts
1,769
Material Chemistry For Sensing & Imaging
1,525
Photochemistry
1,292
Physical Chemistry
618
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
102,587
Articles tracked across the journal lifetime
Indexed publication set
3,634
3,143 cited publications
Last 12 months
1,951
162.6 publications/month
Open access share
12.4%
242 OA publications in the last year
Leading citing country
China
5,995 citing publications
Leading citing field
Synthesis
15,502 citing publications
Latest tracked publication
21 October 2026
10 recent records available
Coverage & Indexing History
v30n1,Jan. 1965-v43n4,Feb. 17, 1978; v65n1,Jan. 14 2000-
v30n1,Jan. 1965-v43n4,Feb. 17, 1978; v65n1,Jan. 14 2000-
Active Coverage
Active Coverage
Research Focus & Classification
Indexed Subjects
Synthesis
Issuing & Sponsoring Bodies
Contributor
American Chemical Society
Broad Categories
Chemistry
Synthesis
MeSH Descriptors
Chemistry, Organic
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1021/acs.joc.6c01936
Open DOI
Palladium-Catalyzed Cascade Heck/C–H Activation for Divergent Synthesis of Functionalized Pyrrolo[2,1- a ]isoquinolinones via Alkyne or Aryne Insertion
Isoquinoline-containing polycyclic skeletons are ubiquitous in bioactive compounds. Introduced in this paper is Pd-catalyzed cascade Heck/C–H activation/cyclative insertion reactions to construct fused pyrroloisoquinolinones. Intramolecu...
02
DOI 10.1021/acs.joc.6c00945
Open DOI
Nickel-Catalyzed C–O Cross-coupling of N -Boc-Protected Amino Alcohols with (Hetero)aryl Halides
The aryloxyalkylamine motif is a privileged pharmacophore found in bioactive molecules. However, achieving its direct and chemoselective construction via O-arylation of amino alcohols remains a significant challenge in synthetic chemistr...
03
DOI 10.1021/acs.joc.6c01627
Open DOI
Electrochemical Trifluoromethylation of Alkenes Using the Unpurified CF3I Reagent from Fluoroform
Fluoroform (HCF3) is an excess industrial gas with a significant greenhouse effect. The utilization of fluoroform as the trifluoromethyl precursor could turn the waste into a value-added product. In this work, we report a protocol for co...
04
DOI 10.1021/acs.joc.6c01343
Open DOI
Stereo- and Chemoselective Conversion of Alkynylphosphonates to Vinyl and Alkyl Phosphonates
A novel strategy for the selective semi-reduction and exhaustive reduction of alkynyl phosphonates to (E)-vinyl phosphonates and alkyl phosphonates, respectively, has been developed using a Zn/NiCl2·6H2O system. The hydrogenation chemose...
05
DOI 10.1021/acs.joc.6c02088
Open DOI
Diastereoselective Synthesis of β-Branched α-Amino Acids from β, γ-Unsaturated Amides and Glycine-Derived Imines via Tandem Isomerization-Conjugate Addition
A base-promoted diastereoselective synthesis of β-branched α-amino acid derivatives is reported, proceeding via tandem isomerization–conjugate addition of β,γ-unsaturated amides with glycine-derived imines under transition-metal-free con...
06
DOI 10.1021/acs.joc.6c01744
Open DOI
Conformational Lability of Bispidine as a Route to New Polycyclic Compounds
In this study, novel tricyclic compounds based on bispidine were prepared via a Michael addition–Henry domino reaction. This reaction sequence proceeds under mild conditions with high diastereoselectivity. Postsynthetic transformation pa...
07
DOI 10.1021/acs.joc.6c01924
Open DOI
Development of a Carbonyl Cyclopentannulation Reagent Based on a 1,4-Dithiane-Fused Nazarov Reaction
Cyclopentanes are common substructures in biologically relevant molecules, but methods for their de novo synthesis from simple building blocks are limited. In this work, we report the development of a novel reagent that allows the direct...
08
DOI 10.1021/acs.joc.6c01934
Open DOI
Sodium Borohydride Reduction of Esters in Toluene Using the All-at-Once Addition Method with an Alcohol Activator
The sodium borohydride (NaBH4) reduction of esters in toluene (also in 2-MeTHF and CPME) has been accomplished using 2-methoxyethanol (2-ME) as an activator. In previous mixed-solvent methods, it was necessary to add methanol dropwise to...
09
DOI 10.1021/acs.joc.6c02174
Open DOI
Further Insights into the Stereoselective Total Synthesis of Ageliferin via Dearomatizing Diels–Alder Cycloaddition
We report the total synthesis of ageliferin, focusing on the preparation of substrate for the D-tartrate-tethered cycloaddition and late-stage transformations. A D-tartrate-derived tether was designed to facilitate a challenging intramol...
10
DOI 10.1021/acs.joc.6c01863
Open DOI
Deciphering the Mechanistic Origin of Divergent Radical Annulation Reactions of ortho -Cyanoaryl Acrylamides
The divergent radical annulation reactions of ortho-cyanoaryl acrylamides involving cyanomethyl and α-oxyalkyl radicals were investigated using density functional theory (DFT) combined with DLPNO-CCSD(T) single-point computations. The ca...
Bibliographical & Catalog Notes
Place of publication varies.
Issues for Jan. 12, 1973- accompanied by: Journal of organic chemistry. Supplementary material, on microfiche; <Mar. 24, 1995-> by supporting information on microfiche.
Available on microfilm from ACS Microfiche Service; also issued online.
Issued by the American Chemical Society, 1955-
Concurrent tables of contents included July 15, 1999- in: Organic letters.
Vol. 55, no. 1 (JAN 1990)19890828 Notice not published Printed on acid-free paper