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Volumn 69, Issue 21, 2004, Pages 7294-7302

Synthesis of spirovetivane sesquiterpenes from santonin. Synthesis of (+)-anhydro-β-rotunol and all diastereomers of 6,11-spirovetivadiene

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYLATION; ISOMERS; ORGANIC CHEMICALS; OXIDATION;

EID: 5444224868     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo040189n     Document Type: Article
Times cited : (41)

References (73)
  • 40
    • 5444261061 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum of 8, lack of selectivity during irradiation prevented determining the stereochemistry of H1 by NOE experiments. The stereochemistry of H1 was determined by NOEs in compound 11.
  • 54
    • 5444257860 scopus 로고
    • For synthesis of racemic anhydro-β-rotunol see: (c) Marx, J. N.; Bih, Q. R. J. Org. Chem. 1987, 52, 336-338.
    • (1987) J. Org. Chem. , vol.52 , pp. 336-338
    • Marx, J.N.1    Bih, Q.R.2
  • 64
    • 5444254852 scopus 로고
    • The structure of solavetivone has been demonstrated through a number of syntheses: (a) Murai, A.; Sato, S.; Masamune, T. Bull. Chem. Soc. Jpn. 1984, 57, 2282-2285.
    • (1984) Bull. Chem. Soc. Jpn. , vol.57 , pp. 2282-2285
    • Murai, A.1    Sato, S.2    Masamune, T.3
  • 73
    • 5444220490 scopus 로고    scopus 로고
    • note
    • We thank professor Chia-Li Wu from Tamkang University for sending us copies of the NMR spectra for natural (-)-agarospirene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.