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Volumn 14, Issue 16, 2012, Pages 4114-4117

{1,6}-transannular catalytic asymmetric Gosteli-Claisen rearrangement

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EID: 84865254140     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol3017676     Document Type: Article
Times cited : (33)

References (37)
  • 34
    • 0000648665 scopus 로고
    • Funk has reported the uncatalyzed {1,6}-transannular Ireland-Claisen rearrangement of an 11-membered lactone containing an E -configured double bond. In the event, the 7-membered rearrangement product was isolated as a mixture of diastereomers (trans / cis = 59:41); see
    • Funk has reported the uncatalyzed {1,6}-transannular Ireland-Claisen rearrangement of an 11-membered lactone containing an E -configured double bond. In the event, the 7-membered rearrangement product was isolated as a mixture of diastereomers (trans / cis = 59:41); see: Abelman, M. M.; Funk, R. L.; Munger, J. D. J. Am. Chem. Soc. 1982, 104, 4030-4032
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4030-4032
    • Abelman, M.M.1    Funk, R.L.2    Munger, J.D.3
  • 37
    • 0034721430 scopus 로고    scopus 로고
    • (Mukaiyama-Michael reaction), and ref 1m (Gosteli-Claisen rearrangement)
    • Evans, D. A.; Rovis, T.; Kozlowski, M. C.; Downey, C. W.; Tedrow, J. S. J. Am. Chem. Soc. 2000, 122, 9134-9142 (Mukaiyama-Michael reaction), and ref 1m (Gosteli-Claisen rearrangement)
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9134-9142
    • Evans, D.A.1    Rovis, T.2    Kozlowski, M.C.3    Downey, C.W.4    Tedrow, J.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.