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Volumn 10, Issue 23, 2008, Pages 5469-5472

Rhodium-complex-catalyzed addition reactions of chloroacetyl chlorides to alkynes

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EID: 61349128452     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol802260w     Document Type: Article
Times cited : (42)

References (32)
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    • (a) Triazole: Prodanchunk, N. G.; Megera, I. V.; Patratii, V. K. Pharm. Chem. J. 1984, 18, 108.
  • 3
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    • Thiazoline: Mirskova, A. N.; Levkovskaya, G. G.; Kalikhman, I. D.; Voronkov, M. G. Zh. Org. Khim. 1979, 15, 2301.
    • (b) Thiazoline: Mirskova, A. N.; Levkovskaya, G. G.; Kalikhman, I. D.; Voronkov, M. G. Zh. Org. Khim. 1979, 15, 2301.
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    • Pyrazole: Levkovskaya, G. G.; Bozhenkov, G. V.; Malyushenko, R. N.; Mirskova, A. N. Russ. J. Org. Chem. 2001, 37, 1795.
    • (c) Pyrazole: Levkovskaya, G. G.; Bozhenkov, G. V.; Malyushenko, R. N.; Mirskova, A. N. Russ. J. Org. Chem. 2001, 37, 1795.
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    • Isoxazole: Aliev, A. G. Russ. J. Org. Chem. 2005, 41, 1192.
    • (f) Isoxazole: Aliev, A. G. Russ. J. Org. Chem. 2005, 41, 1192.
  • 9
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    • Thiophene: Alberola, A.; Andres, J. M.; Gonzalez, A.; Pedrosa, R.; Pradanos, P. Synth. Commun. 1990, 20, 2537.
    • (h) Thiophene: Alberola, A.; Andres, J. M.; Gonzalez, A.; Pedrosa, R.; Pradanos, P. Synth. Commun. 1990, 20, 2537.
  • 23
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    • and references cited therein. A formal CO retentive reaction of aroyl chlorides with norbornene, which proceeds through decarbonylation-carbonylation processes, has been reported. See
    • A formal CO retentive reaction of aroyl chlorides with norbornene, which proceeds through decarbonylation-carbonylation processes, has been reported. See: Sugihara, T.; Satoh, T.; Miura, M.; Nomura, M. Adv. Synth. Catal. 2004, 346, 1765, and references cited therein.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1765
    • Sugihara, T.1    Satoh, T.2    Miura, M.3    Nomura, M.4
  • 25
    • 61349085906 scopus 로고    scopus 로고
    • α-Halo ketones are also useful intermediates in organic synthesis. See: (a) Sci. Synth. 2005, 26, 869.
    • α-Halo ketones are also useful intermediates in organic synthesis. See: (a) Sci. Synth. 2005, 26, 869.
  • 26
    • 61349116611 scopus 로고    scopus 로고
    • (b) Sci. Synth. 2005, 26, 745.
    • (2005) Synth , vol.26 , pp. 745
    • Sci1
  • 27
    • 61349101643 scopus 로고    scopus 로고
    • For X-ray crystallographic details, see the Supporting Information
    • For X-ray crystallographic details, see the Supporting Information.
  • 28
    • 61349098667 scopus 로고    scopus 로고
    • For details, see the Supporting Information
    • For details, see the Supporting Information.
  • 29
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    • Details will be reported separately
    • Details will be reported separately.
  • 31
    • 61349126014 scopus 로고    scopus 로고
    • 3MeNCl, although the reaction was messy. For details, see the Supporting Information.
    • 3MeNCl, although the reaction was messy. For details, see the Supporting Information.
  • 32
    • 61349197334 scopus 로고    scopus 로고
    • Lu, X. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; II, pp 2267-2287. (14) For γ-alkylidenebutenolides in pharmaceutical applications, see: Ahmed, Z.; Langer, P. J. Org. Chem. 2004, 69, 3753, and references cited therein.
    • Lu, X. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2267-2287. (14) For γ-alkylidenebutenolides in pharmaceutical applications, see: Ahmed, Z.; Langer, P. J. Org. Chem. 2004, 69, 3753, and references cited therein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.