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Volumn 45, Issue 10, 2004, Pages 2227-2229

Asymmetric syntheses of (1R,1′R,5′R,7′R) and (1S,1′R,5′R,7′R)-1-hydroxy-exo-brevicomin and a formal synthesis of (+)-exo-brevicomin

Author keywords

[No Author keywords available]

Indexed keywords

BREVICOMIN; PHEROMONE; PICOLINIC ACID;

EID: 1242295356     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.12.157     Document Type: Article
Times cited : (15)

References (30)
  • 7
    • 0000119097 scopus 로고
    • For earlier reported syntheses see:
    • For earlier reported syntheses see: Mori K. Tetrahedron. 45:1989;3233-3298.
    • (1989) Tetrahedron , vol.45 , pp. 3233-3298
    • Mori, K.1
  • 11
    • 0141888361 scopus 로고    scopus 로고
    • For some recent syntheses see:
    • For some recent syntheses see: Raghavan S., Joseph S.C. Tetrahedron Lett. 44:2003;8237-8239.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 8237-8239
    • Raghavan, S.1    Joseph, S.C.2
  • 25
    • 0037124555 scopus 로고    scopus 로고
    • and references cited therein
    • Carlo B., Giuliana R. Tetrahedron. 58:2002;4981-5021. and references cited therein.
    • (2002) Tetrahedron , vol.58 , pp. 4981-5021
    • Carlo, B.1    Giuliana, R.2
  • 26
    • 85030906891 scopus 로고    scopus 로고
    • note
    • Spectral data for selected compounds:
  • 30
    • 85030894422 scopus 로고    scopus 로고
    • note
    • 3)} using a Chiracel OD-H column. (For 8a 10% i-propanol/n-hexane, flow rate 0.5 mL/min, λ=254 nm; for 11a 7% i-propanol/n-hexane, flow rate 0.5 mL/min, λ=254 nm.).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.