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Volumn 7, Issue 14, 2005, Pages 3103-3106

Stereoselective intramolecular 1,3 C-H insertion in Rh(II) carbene reactions

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EID: 22244490671     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051130l     Document Type: Article
Times cited : (35)

References (40)
  • 4
    • 0029026470 scopus 로고
    • For examples of Rh(II) carbene mediated intramolecular C-H insertion in organic synthesis, see: (a) Taber, D. F.; You, K. K. J. Am. Chem. Soc. 1995, 117, 5757-5762.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5757-5762
    • Taber, D.F.1    You, K.K.2
  • 12
    • 33845374322 scopus 로고
    • For mechanistic investigations on Rh(II) carbene C-H insertions, see: (a) Taber, D. F.; Ruckle, R. E., Jr. J. Am. Chem. Soc. 1986, 108, 7686-7693.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 7686-7693
    • Taber, D.F.1    Ruckle Jr., R.E.2
  • 31
    • 0346429531 scopus 로고
    • 1,3 G-H insertion was reported in the Cu-catalyzed reaction of a structurally rigid diazo compound: Yates, P.; Danishefsky, S. J. Am. Chem. Soc. 1962, 84, 879-880.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 879-880
    • Yates, P.1    Danishefsky, S.2
  • 39
    • 32744474159 scopus 로고    scopus 로고
    • note
    • 1H NMR (400 MHz). For the 1,5 insertion product, there are two stereoisomers.
  • 40
    • 0036068448 scopus 로고    scopus 로고
    • For a discussion on the conformation of α-diazo carbonyl compounds, see: Kirmse, W. Eur. J. Org. Chem. 2002, 2193-2256.
    • (2002) Eur. J. Org. Chem. , pp. 2193-2256
    • Kirmse, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.