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Volumn , Issue 12, 1997, Pages 1475-1480

New synthesis of 2,6-diaryl-4-oxo-3,7-dioxabicyclo[3.3.0]octanes: Syntehsis of (±)-styraxin

Author keywords

2,6 Diaryl 4 oxo 3,7 dioxabicyclo 3.3.0 octane; Furofuran; Lignan; Stereocontrolled aldol reaction; Styraxin

Indexed keywords

2,6 DIARYL 4 OXO 3,7 DIOXABICYCLO(3.3.0.)OCTANE; ALDEHYDE; LIGNAN; OCTANE; STYRAXIN; SUCCINIC ANHYDRIDE; UNCLASSIFIED DRUG;

EID: 0031468007     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-1375     Document Type: Article
Times cited : (9)

References (26)
  • 2
    • 0004266767 scopus 로고
    • Cambridge University Press: Cambridge
    • (b) Ayres, D.C.; Loike, J.D. Lignans; Cambridge University Press: Cambridge, 1990.
    • (1990) Lignans
    • Ayres, D.C.1    Loike, J.D.2
  • 22
    • 84889191638 scopus 로고    scopus 로고
    • note
    • A synthesis of 1 based on the oxidative coupling of a cinnamic acid derivative and a cinnamic alcohol derivative has been reported by Cooper et al. However, their method gave the desired monolactone as a mixture with the corresponding 2 and 3.
  • 24
    • 37049070735 scopus 로고
    • A synthesis of (±)-styraxin (1a) based on intramolecular Mukaiyama aldol reaction has been reported by Stevens et al. However, the key reaction was low yielding and poorly stereoselective. Stevens, D.R.; Till, C.P.; Whiting, D.A. J. Chem. Soc., Perkin Trans. 1 1992, 185.
    • (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 185
    • Stevens, D.R.1    Till, C.P.2    Whiting, D.A.3
  • 25
    • 84889212416 scopus 로고    scopus 로고
    • note
    • The anti-isomer of 9 was also obtained as a minor product in 6 % yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.