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Volumn 53, Issue 49, 1997, Pages 16789-16794

Media controlled photo - Favorskii type rearrangement of α-chloro acetophenones: Synthesis of phenylacetic acids

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ACETONITRILE; ACETOPHENONE DERIVATIVE; METHANOL; PHENYLACETIC ACID DERIVATIVE; PROPYLENE OXIDE; SOLVENT;

EID: 0030731319     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)10081-3     Document Type: Article
Times cited : (19)

References (47)
  • 1
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    • and references cited therein
    • (a) Shen, T. Y Angew. Chem. Int. Ed. Engl. 1972, 11, 460, and references cited therein;
    • (1972) Angew. Chem. Int. Ed. Engl. , vol.11 , pp. 460
    • Shen, T.Y.1
  • 15
    • 0000962954 scopus 로고
    • John Wiley, New York
    • Kende, A. S. Organic reactions, John Wiley, New York, 1960, 11, 261.
    • (1960) Organic Reactions , vol.11 , pp. 261
    • Kende, A.S.1
  • 28
    • 84984281414 scopus 로고
    • For the preparation of 1a-f see: Kajigaeshi, S.; Kakinami, T.; Moriwaki, M.; Fujisaki, S.; Maeno, K.; Okamoto, T. Synthesis, 1988, 545; for 1i see: Hicter, M. I.; Boucherle, A. Bull. Soc. Chim. France, 1965, 11, 3334; for 1h see: Nardi, D.; Tajana, A.; Leonard, A.; Penini, R.; Portioli, F.; Magistretti, M. Subissi, A. J. Med. Chem., 1981, 24, 727; for 1j see Adams, R.; Theobald, C. W. J. Am. Chem. soc., 1943, 65, 2208.
    • (1988) Synthesis , pp. 545
    • Kajigaeshi, S.1    Kakinami, T.2    Moriwaki, M.3    Fujisaki, S.4    Maeno, K.5    Okamoto, T.6
  • 29
    • 17544387212 scopus 로고
    • For the preparation of 1a-f see: Kajigaeshi, S.; Kakinami, T.; Moriwaki, M.; Fujisaki, S.; Maeno, K.; Okamoto, T. Synthesis, 1988, 545; for 1i see: Hicter, M. I.; Boucherle, A. Bull. Soc. Chim. France, 1965, 11, 3334; for 1h see: Nardi, D.; Tajana, A.; Leonard, A.; Penini, R.; Portioli, F.; Magistretti, M. Subissi, A. J. Med. Chem., 1981, 24, 727; for 1j see Adams, R.; Theobald, C. W. J. Am. Chem. soc., 1943, 65, 2208.
    • (1965) Bull. Soc. Chim. France , vol.11 , pp. 3334
    • Hicter, M.I.1    Boucherle, A.2
  • 30
    • 0019411165 scopus 로고
    • For the preparation of 1a-f see: Kajigaeshi, S.; Kakinami, T.; Moriwaki, M.; Fujisaki, S.; Maeno, K.; Okamoto, T. Synthesis, 1988, 545; for 1i see: Hicter, M. I.; Boucherle, A. Bull. Soc. Chim. France, 1965, 11, 3334; for 1h see: Nardi, D.; Tajana, A.; Leonard, A.; Penini, R.; Portioli, F.; Magistretti, M. Subissi, A. J. Med. Chem., 1981, 24, 727; for 1j see Adams, R.; Theobald, C. W. J. Am. Chem. soc., 1943, 65, 2208.
    • (1981) J. Med. Chem. , vol.24 , pp. 727
    • Nardi, D.1    Tajana, A.2    Leonard, A.3    Penini, R.4    Portioli, F.5    Magistretti, M.6    Subissi, A.7
  • 31
    • 0343262822 scopus 로고
    • For the preparation of 1a-f see: Kajigaeshi, S.; Kakinami, T.; Moriwaki, M.; Fujisaki, S.; Maeno, K.; Okamoto, T. Synthesis, 1988, 545; for 1i see: Hicter, M. I.; Boucherle, A. Bull. Soc. Chim. France, 1965, 11, 3334; for 1h see: Nardi, D.; Tajana, A.; Leonard, A.; Penini, R.; Portioli, F.; Magistretti, M. Subissi, A. J. Med. Chem., 1981, 24, 727; for 1j see Adams, R.; Theobald, C. W. J. Am. Chem. soc., 1943, 65, 2208.
    • (1943) J. Am. Chem. Soc. , vol.65 , pp. 2208
    • Adams, R.1    Theobald, C.W.2
  • 33
    • 0442283671 scopus 로고
    • For the first report on photolysis of substituted α-chloro acetophenones in methanol see: Anderson, J. C.; Reese, C. B. Tetrahedron Lett. 1962, 1, 1. Our results are parallel with this report.
    • (1962) Tetrahedron Lett. , vol.1 , pp. 1
    • Anderson, J.C.1    Reese, C.B.2
  • 34
    • 85036679829 scopus 로고    scopus 로고
    • Our attempts to optimise the yields of phenylacetic acids by increasing the percentage of water contents (upto 20%) in 1,4-dioxane, acetone or acetonitrile gave identical results
    • Our attempts to optimise the yields of phenylacetic acids by increasing the percentage of water contents (upto 20%) in 1,4-dioxane, acetone or acetonitrile gave identical results.
  • 37
    • 0008477958 scopus 로고
    • for 2j see: ref. 7d
    • 1H NMR data of substituted acetophenones 2a-i and chlorobenzene derivatives see: Pouchert, C. J. The Aldrich Library of NMR spectra, Aldrich Chemical Company, Wisconsia; for 2g see: Baddeley, G.; Wrencil, E. J. Chem. Soc., 1956, 4943; for 2j see: ref. 7d.
    • (1956) J. Chem. Soc. , pp. 4943
    • Baddeley, G.1    Wrencil, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.