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Volumn 10, Issue 7, 2008, Pages 1425-1428

Rhodium(II)-catalyzed transylidation of aryliodonium ylides: Electronic effects of aryl groups determine their thermodynamic stabilities

Author keywords

[No Author keywords available]

Indexed keywords

IODINATED HYDROCARBON; RHODIUM;

EID: 45849140576     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800211x     Document Type: Article
Times cited : (24)

References (27)
  • 1
  • 6
    • 11144356233 scopus 로고    scopus 로고
    • Reviews: a
    • Reviews: (a) Muller, P. Acc. Chem. Res. 2004, 37, 243.
    • (2004) Acc. Chem. Res , vol.37 , pp. 243
    • Muller, P.1
  • 9
    • 59849128909 scopus 로고
    • Supplement D, Patai S, Rappoport. Z, Eds, Wiley: New York, Chapter 18
    • (d) Koser, G. F. In The Chemistry of Functional Groups, Supplement D.; Patai S., Rappoport. Z., Eds.; Wiley: New York, 1983; Chapter 18.
    • (1983) The Chemistry of Functional Groups
    • Koser, G.F.1
  • 18
    • 39549092429 scopus 로고    scopus 로고
    • Recently, we reported the intermolecular transfer of the alkylidene groups of arylbromonium ylides to aryl halides (iodides, bromides, and chlorides) yielding a variety of aryliodonium, bromonium, and chloronium ylides under thermal or metal-catalyzed conditions. See: Ochiai, M.; Tada, N.; Okada, T.; Sota, A.; Miyamoto, K. J. Am. Chem. Soc. 2008, 130, 2118.
    • Recently, we reported the intermolecular transfer of the alkylidene groups of arylbromonium ylides to aryl halides (iodides, bromides, and chlorides) yielding a variety of aryliodonium, bromonium, and chloronium ylides under thermal or metal-catalyzed conditions. See: Ochiai, M.; Tada, N.; Okada, T.; Sota, A.; Miyamoto, K. J. Am. Chem. Soc. 2008, 130, 2118.
  • 20
    • 33947086188 scopus 로고
    • For transylidations between a diazo compound and a halonium ylide, see: a
    • For transylidations between a diazo compound and a halonium ylide, see: (a) Sheppard, W. A.; Webster, O. W. J. Am. Chem. Soc. 1973, 95, 2695.
    • (1973) J. Am. Chem. Soc , vol.95 , pp. 2695
    • Sheppard, W.A.1    Webster, O.W.2
  • 23
    • 59849111779 scopus 로고    scopus 로고
    • For instance, p-nitrophenyliodonium dinitromethylide is more stable to thermal decomposition than phenyliodonium dinitromethylide, but the reverse is true for the iodonium ylides derived from dimedone. See Ref 4d.
    • For instance, p-nitrophenyliodonium dinitromethylide is more stable to thermal decomposition than phenyliodonium dinitromethylide, but the reverse is true for the iodonium ylides derived from dimedone. See Ref 4d.
  • 25
    • 0038445018 scopus 로고    scopus 로고
    • Wirth, T, Ed, Springer: Berlin
    • Ochiai, M. In Topics in Current Chemistry; Wirth, T., Ed.; Springer: Berlin, 2003; Vol. 224, p 5.
    • (2003) Topics in Current Chemistry , vol.224 , pp. 5
    • Ochiai, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.