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Volumn 37, Issue 7, 2008, Pages 770-771

Stereocontrolled total synthesis of (-)-gleenol using Claisen rearrangement of sterically congested dihydropyran

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EID: 49149110593     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2008.770     Document Type: Article
Times cited : (6)

References (24)
  • 8
    • 0032356950 scopus 로고    scopus 로고
    • For the synthesis of (-)-1, see: a) S. Ohira, N. Yoshihara, T. Hasegawa, Chem. Lett. 1998, 739.
    • For the synthesis of (-)-1, see: a) S. Ohira, N. Yoshihara, T. Hasegawa, Chem. Lett. 1998, 739.
  • 15
    • 0000226513 scopus 로고    scopus 로고
    • For the pioneering work of the synthesis of spirocycles by Claisen rearrangement of bicyclic dihydropyrans, see: R. E. Ireland, P. A. Aristoff, J. Org. Chem. 1979, 44, 4323
    • For the pioneering work of the synthesis of spirocycles by Claisen rearrangement of bicyclic dihydropyrans, see: R. E. Ireland, P. A. Aristoff, J. Org. Chem. 1979, 44, 4323.
  • 20
    • 33646568495 scopus 로고    scopus 로고
    • 2,3 coupling constants of ≥7.0Hz. For detail, see: M. Cheeseman, S. D. Bull, Synlett 2006, 1119, and references therein.
    • 2,3 coupling constants of ≥7.0Hz. For detail, see: M. Cheeseman, S. D. Bull, Synlett 2006, 1119, and references therein.
  • 23
    • 49149093358 scopus 로고    scopus 로고
    • Although the relative stereochemistry of 12 was not determined at this point, the stereochemistry was eventually assigned by leading to, -1
    • Although the relative stereochemistry of 12 was not determined at this point, the stereochemistry was eventually assigned by leading to (-)-1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.