Here, we report the intramolecular Heck cross-coupling of 1,3-dienylphosphonates, affording unique and regioselective access to unprecedented benzofused phostone and phostam derivatives. The reactions proceeded under operationally simple and mild conditions with a wide substrate scope.
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http://dx.doi.org/10.1021/acsomega.4c06616 | DOI Listing |
ACS Omega
November 2024
Faculty of Sciences of Bizerte, LR18ES11, Laboratory of Hetero-Organic Compounds and Nanostructured Materials, University of Carthage, Bizerte 7021, Tunisia.
Here, we report the intramolecular Heck cross-coupling of 1,3-dienylphosphonates, affording unique and regioselective access to unprecedented benzofused phostone and phostam derivatives. The reactions proceeded under operationally simple and mild conditions with a wide substrate scope.
View Article and Find Full Text PDFBeilstein J Org Chem
May 2023
State Key Laboratory of Chemical Resource Engineering, Department of Organic Chemistry, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China.
Phostams, phostones, and phostines are a series of 1,2-azaphosphaheterocycle and 1,2-oxaphosphaheterocycle 2-oxide derivatives. They are phosphorus analogues of lactams and lactones and important biologically active compounds. The strategies for the synthesis of medium and large phostams, phostones, and phostines are summarized.
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