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150 related items for PubMed ID: 35605977

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  • 6. Photocatalyzed Triplet Sensitization of Oximes Using Visible Light Provides a Route to Nonclassical Beckmann Rearrangement Products.
    Zhang X, Rovis T.
    J Am Chem Soc; 2021 Dec 22; 143(50):21211-21217. PubMed ID: 34905347
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  • 7. Radical addition to oxime ethers for asymmetric synthesis of beta-amino acid derivatives.
    Miyabe H, Fujii K, Naito T.
    Org Biomol Chem; 2003 Jan 21; 1(2):381-90. PubMed ID: 12929434
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  • 10. The oxime portmanteau motif: released heteroradicals undergo incisive EPR interrogation and deliver diverse heterocycles.
    Walton JC.
    Acc Chem Res; 2014 Apr 15; 47(4):1406-16. PubMed ID: 24654991
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  • 11. Chemodivergent Synthesis of Oxazoles and Oxime Ethers Initiated by Selective C-N/C-O Formation of Oximes and Diazo Esters.
    Qi Z, Wang S.
    Org Lett; 2021 Nov 05; 23(21):8549-8553. PubMed ID: 34618474
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  • 13. Visible-Light-Promoted Selenocyanation of Cyclobutanone Oxime Esters Using Potassium Selenocyanate.
    Zhao X, Ji L, Gao Y, Sun T, Qiao J, Li A, Lu K.
    J Org Chem; 2021 Sep 03; 86(17):11399-11406. PubMed ID: 34365792
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  • 18. Oxime Ether Synthesis through O-H Functionalization of Oximes with Diazo Esters under Blue LED Irradiation.
    Li Q, Cai BG, Li L, Xuan J.
    Org Lett; 2021 Sep 03; 23(17):6951-6955. PubMed ID: 34382794
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  • 20. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.
    Tollefson EJ, Hanna LE, Jarvo ER.
    Acc Chem Res; 2015 Aug 18; 48(8):2344-53. PubMed ID: 26197033
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