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ChemRxiv (pronounced "chem archive"—the X represents the Greek letter chi [χ]) is an open access preprint archive for chemistry. [1] It is operated by the American Chemical Society, Royal Society of Chemistry [2] and German Chemical Society. [3] [4] The new preprint server was announced already in 2016, [5] [6] but was only opened online in ...
ChemRxiv [10] Chemistry: Open access preprint archive for chemistry >10,000 2017 American Chemical Society, Royal Society of Chemistry & German Chemical Society: ChinaXiv: Multidisciplinary: Preprint server for interdisciplinary research in China >10,000 2016 National Science Library, Chinese Academy of Sciences: CogPrints: Multidisciplinary
Typical publishing workflow for an academic journal article (preprint, postprint, and published) with open access sharing rights per SHERPA/RoMEO.In academic publishing, a preprint is a version of a scholarly or scientific paper that precedes formal peer review and publication in a peer-reviewed scholarly or scientific journal.
Not-for-profit servers (e.g. arXiv, bioRxiv, chemRxiv, medRxiv) Unrestricted When posting the preprint, authors should choose a CC BY-NC-ND license [62] National Academy of Sciences: Unrestricted Unrestricted Unrestricted [63] [64] [65] Optica: Unrestricted Unrestricted Unrestricted [66] Oxford University Press: Unrestricted, except:
ACS also created ChemRxiv, which is an open access preprint repository for the chemical sciences, co-owned, and collaboratively managed by the American Chemical Society (ACS), German Chemical Society (GDCh), Royal Society of Chemistry (RSC), the chemistry community, other societies, funders, and non-profits; open for submissions and available ...
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Kenneth M. Merz Jr. is an American biochemist and molecular biologist currently the Joseph Zichis Chair and a distinguished university professor at Michigan State University and editor-in-chief of American Chemical Society's Journal of Chemical Information and Modeling.
In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R').