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New approach to .alpha.-keto esters

Cite this: J. Org. Chem. 1973, 38, 20, 3653–3654
Publication Date (Print):October 1, 1973
https://doi.org/10.1021/jo00960a057
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    Cited By

    This article is cited by 20 publications.

    1. Ganapati D. Yadav and, Ramesh D. Bhagat. Synthesis of Methyl Phenyl Glyoxylate via Clean Oxidation of Methyl Mandelate over a Nanocatalyst Based on Heteropolyacid Supported on Clay. Organic Process Research & Development 2004, 8 (6) , 879-882. https://doi.org/10.1021/op049858p
    2. Xian Huang,, Dehui Duan, and, Weixin Zheng. Studies on Hydrozirconation of 1-Alkynyl Sulfoxides or Sulfones and the Application for the Synthesis of Stereodefined Vinyl Sulfoxides or Sulfones. The Journal of Organic Chemistry 2003, 68 (5) , 1958-1963. https://doi.org/10.1021/jo0111154
    3. Majid M. Heravi, Fatemeh F. Bamoharram. Applications of heteropoly acids in industry. 2022, 305-373. https://doi.org/10.1016/B978-0-323-88441-9.00005-3
    4. Tse‐Lok Ho, Mary Fieser, Rick Danheiser, William Roush, Janice Smith, Louis Fieser. Ozone. 2013, 336-336. https://doi.org/10.1002/9780471264194.fos07546.pub4
    5. Ross M. Denton, Jie An, Petra Lindovska, William Lewis. Phosphonium salt-catalysed synthesis of nitriles from in situ activated oximes. Tetrahedron 2012, 68 (13) , 2899-2905. https://doi.org/10.1016/j.tet.2012.01.067
    6. Tse‐Lok Ho, Mary Fieser, Rick Danheiser, William Roush, Janice Smith, Louis Fieser. Ozone. 2010, 000-000. https://doi.org/10.1002/9780471264194.fos07546.pub3
    7. Tse‐Lok Ho, Mary Fieser, Rick Danheiser, William Roush, Janice Smith, Louis Fieser. Ozone. 2009, 000-000. https://doi.org/10.1002/9780471264194.fos07546.pub2
    8. Tse‐Lok Ho, Mary Fieser, Rick Danheiser, William Roush, Janice Smith, Louis Fieser. Ozone. 2006https://doi.org/10.1002/9780471264194.fos07546
    9. Gui-Sheng Zhang, Hui Gong. A General and Simple Synthesis of Phenylglyoxylic Esters via the Oxidation of Mandelic Esters with Ammonium Chlorochromate Adsorbed on Alumina. Synthetic Communications 1999, 29 (18) , 3149-3153. https://doi.org/10.1080/00397919908085939
    10. Zbigniew Pakulski, Aleksander Zamojski. Diastereoselective propargylation of sugar aldehydes. New synthesis of 6-deoxyheptoses. Tetrahedron 1997, 53 (7) , 2653-2666. https://doi.org/10.1016/S0040-4020(96)01156-8
    11. Derek H.R. Barton, Ching-Yuh Chern, Joseph Cs. Jaszberenyi. The invention of radical reactions. Part XXXIV. Homologation of carboxylic acids to α-keto carboxylic acids by Barton-ester based radical chain chemistry. Tetrahedron 1995, 51 (7) , 1867-1886. https://doi.org/10.1016/0040-4020(94)01054-4
    12. Lajos Kovács. Methods for the synthesis of α‐keto esters. Recueil des Travaux Chimiques des Pays-Bas 1993, 112 (9) , 471-496. https://doi.org/10.1002/recl.19931120902
    13. . The synthesis of carboxylic acids and esters and their derivatives. 1991, 1-224. https://doi.org/10.1002/9780470772423.ch1
    14. Philip C Bulman Page, Stephen Rosenthal. Simple preparation of α-bromo acyl silanes α-ketoacyl silanes and α-ketoesters from silyl acetylenes. Tetrahedron 1990, 46 (7) , 2573-2586. https://doi.org/10.1016/S0040-4020(01)82037-8
    15. Philip C. Bulman Page, Stephen Rosenthal. A simple and general synthesis of α-keto esters. Tetrahedron Letters 1986, 27 (17) , 1947-1950. https://doi.org/10.1016/S0040-4039(00)84419-6
    16. Alan H. Haines. Alkynes. 1985, 153-172. https://doi.org/10.1016/B978-0-12-315501-6.50011-9
    17. Paul Müller, José Godoy. Ru-catalyzed oxidation of substituted acetylenes to α-keto esters and α-keto amides with iodosylbenzene. Tetrahedron Letters 1982, 23 (36) , 3661-3664. https://doi.org/10.1016/S0040-4039(00)88651-7
    18. Shigemi Mukaiyama, Junji Inanaga, Masaru Yamaguchi. 4-Dimethylaminopyridine N -Oxide as an Efficient Oxidizing Agent for Alkyl Halides. Bulletin of the Chemical Society of Japan 1981, 54 (7) , 2221-2222. https://doi.org/10.1246/bcsj.54.2221
    19. S. CACCHI, L. CAGLIOTI, P. ZAPPELLI. ChemInform Abstract: A NEW APPROACH TO ALPHA‐KETO ESTERS. Chemischer Informationsdienst 1974, 5 (3) https://doi.org/10.1002/chin.197403212
    20. . Preparation of Difunctional Compounds. 1974, 214-437. https://doi.org/10.1002/9780470125953.ch15

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