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Volumn 128, Issue 49, 2006, Pages 15598-15599

Erratum: Withdrawal of "rhodium-catalyzed arylative and alkenylative cyclization of 1,5-enynes induced by geminal carbometalation of alkynes" (Journal of the American Chemical Society (2006) 128 (15598-15599) DOI: 10.1021/ja067125+);Rhodium-catalyzed arylative and alkenylative cyclization of 1,5-enynes induced by geminal carbometalation of alkynes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUP; ALKYNE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; RHODIUM;

EID: 33845394260     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja310385q     Document Type: Erratum
Times cited : (40)

References (26)
  • 1
    • 0000633011 scopus 로고
    • For reviews, see: Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
    • For reviews, see: (a) Heck, R. F. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 833-864.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 833-864
    • Heck, R.F.1
  • 13
    • 24644468109 scopus 로고    scopus 로고
    • For a related endo-selective hydrative cyclization, see: Chen, Y.; Ho, D. M.; Lee, C. J. Am. Chem. Soc. 2005, 127, 12184.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 12184
    • Chen, Y.1    Ho, D.M.2    Lee, C.3
  • 16
    • 33845452077 scopus 로고    scopus 로고
    • note
    • No reaction occurred at 23 °C, while extensive decomposition of enyne 1 was observed at 60 °C.
  • 22
    • 33845449273 scopus 로고    scopus 로고
    • note
    • (9) The 2-phenyl-1,3-dioxa-2-borinane was chosen instead of phenylboronic acid to avoid proton scrambling.
  • 23
    • 33845436938 scopus 로고    scopus 로고
    • note
    • The isotopic composition remained constant upon resubjection of 8′ to the same reaction conditions for 2 h. In a separate control experiment employing unlabeled 8, no deuterium incorporation was observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.