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The Journal of Organic Chemistry is a peer-reviewed journal published by American Chemical Society, covering Asymmetric Synthesis and Catalysis, Catalytic C–H Functionalization Methods, Chemical Synthesis and Analysis. Over its lifetime it has published 103,263 papers, which have received 3,323,588 citations.
| Publisher | American Chemical Society |
|---|---|
| Reference style | Superscript numbered (ACS) Superscript — small raised numerals in the text (1) Smith, A.; Jones, B.; Lee, C. A Representative Article Title. The Journal of Organic Chemistry 2023, 12, 45–58.
Formats any DOI in The Journal of Organic Chemistry style. No sign-up. |
| Publishes research in | Asymmetric Synthesis and Catalysis Catalytic C–H Functionalization Methods Chemical Synthesis and Analysis Synthetic Organic Chemistry Methods Chemical Reaction Mechanisms |
| ISSN | 0022-3263 |
| Citation impact (2-yr) | 3.38 |
| h-index | 311 |
| i10-index | 75,677 |
| Top institutions publishing here | Centre National de la Recherche Scientifique |
| Journal website | pubs.acs.org |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
The cycloaddition of azides to alkynes is one of the most important synthetic routes to 1H-[1,2,3]-triazoles. Here a novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported. Primary, secondary, and tertiary alkyl azides, aryl azides, and an azido sugar were used successfully in the copper(I)-catalyzed cycloaddition producing diversely 1,4-substituted [1,2,3]-triazoles…
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRapid chromatographic technique for preparative separations with moderate resolutionW. Clark Still, Michael Kahn, and Abhijit MitraCite this: J. Org. Chem. 1978, 43, 14, 2923–2925Publication Date (Print):July 1, 1978Publication History Published online1 May 2002Published inissue 1 July 1978https://doi.org/10.1021/jo00408a041RIGHTS & PERMISSIONSArticle Views50070Altmetric-Citations5333LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article…
ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTNMR Chemical Shifts of Common Laboratory Solvents as Trace ImpuritiesHugo E. Gottlieb, Vadim Kotlyar, and Abraham NudelmanView Author Information Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, IsraelCite this: J. Org. Chem. 1997, 62, 21, 7512–7515Publication Date (Web):October 17, 1997Publication History Received27 June 1997Published online17 October 1997Published inissue 1 October 1997https://pubs.acs.org/doi/10.1021/jo971176vhttps://doi.org/10.1021/jo971176vbrief-reportACS PublicationsCopyright ©…
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTLinear solvation energy relationships. 23. A comprehensive collection of the solvatochromic parameters, .pi.*, .alpha., and .beta., and some methods for simplifying the generalized solvatochromic equationMortimer J. Kamlet, Jose Luis M. Abboud, Michael H. Abraham, and R. W. TaftCite this: J. Org. Chem. 1983, 48, 17, 2877–2887Publication Date (Print):August 1, 1983Publication History Published…
In recent years, photoredox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activation of small molecules. In a general sense, these approaches rely on the ability of metal complexes and organic dyes to convert visible light into chemical energy by engaging in single-electron transfer with organic substrates, thereby…
