Hydrogenation streamlines cyclolignan synthesis

Hydrogenation streamlines cyclolignan synthesis

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Enantioselective hydrogenation is a stalwart reaction in synthetic chemistry. Now, hydrogenation of tetrasubstituted 1,2-dihydronaphthalene esters gives access to more than 30 cyclolignan


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Read our FAQs * Contact customer support REFERENCES * Atanasov, A. G., Zotchev, S. B. & Dirsch, V. M. & the International Natural Product Sciences Taskforce & Supuran, C. T.


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Roberts, N. K. & Bosnich, B. _J. Am. Chem. Soc._ 103, 2273–2280 (1981). Article  CAS  Google Scholar  Download references AUTHOR INFORMATION Author notes * Twitter: @SarlahLab AUTHORS


AND AFFILIATIONS * Department of Chemistry, University of Illinois at Urbana−Champaign, Urbana, IL, USA David B. Ryffel & David Sarlah * Carl R. Woese Institute for Genomic Biology,


University of Illinois at Urbana–Champaign, Urbana, IL, USA David B. Ryffel & David Sarlah Authors * David B. Ryffel View author publications You can also search for this author inPubMed


 Google Scholar * David Sarlah View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to David Sarlah. ETHICS DECLARATIONS


COMPETING INTERESTS The authors declare no competing interests. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Ryffel, D.B., Sarlah, D. Hydrogenation


streamlines cyclolignan synthesis. _Nat. Synth_ 3, 937–938 (2024). https://doi.org/10.1038/s44160-024-00592-8 Download citation * Published: 09 July 2024 * Issue Date: August 2024 * DOI:


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