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Volumn 130, Issue 22, 2008, Pages 6924-6925

Rhodium(I)-catalyzed cycloisomerizations of bicyclobutanes

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE; ALKENE; ALKYNE; AZEPINE DERIVATIVE; BICYCLO COMPOUND; BICYCLO[1.1.0]BUTANE; BUTANE; CARBENE; PROLINE DERIVATIVE; RHODIUM;

EID: 44449087994     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja802906k     Document Type: Article
Times cited : (60)

References (37)
  • 20
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    • (a) Dauben, W. G., Jr J. Am. Chem. Soc. 1972, 94, 3669.
    • (1972) Jr J , vol.94 , pp. 3669
    • Dauben, W.G.1
  • 22
    • 0041878773 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Davies, H. M. L.; Beckwith, R. E. J. Chem. Rev. 2003, 103, 2861.
    • (2003) Chem. Rev , vol.103 , pp. 2861
    • Davies, H.M.L.1    Beckwith, R.E.J.2
  • 27
    • 44449099157 scopus 로고    scopus 로고
    • See Supporting Information for additional optimization conditions
    • (a) See Supporting Information for additional optimization conditions.
  • 28
    • 44449163940 scopus 로고    scopus 로고
    • 1H NMR analysis of a crude reaction mixture. The relative configuration was determined by NOESY (2) or X-ray analysis of the corresponding ketone (3). For details, see Supporting Information.
    • 1H NMR analysis of a crude reaction mixture. The relative configuration was determined by NOESY (2) or X-ray analysis of the corresponding ketone (3). For details, see Supporting Information.
  • 31
    • 44449143450 scopus 로고    scopus 로고
    • Isomerization of N-sulfonamides (no allyl substituents) under conditions favoring formation of 12 or 13 afforded only diene products.
    • Isomerization of N-sulfonamides (no allyl substituents) under conditions favoring formation of 12 or 13 afforded only diene products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.