메뉴 건너뛰기




Volumn 3, Issue 1, 2001, Pages 107-109

Synthesis of the cyclohexan subunit of baconipyrones a and b from furan

Author keywords

[No Author keywords available]

Indexed keywords

BACONIPYRONE A; BACONIPYRONE B; BACONIPYRONE C; CYCLOHEXANE DERIVATIVE; FURAN DERIVATIVE; PYRONE DERIVATIVE; SULFONE;

EID: 0035843286     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol000334t     Document Type: Article
Times cited : (40)

References (16)
  • 4
    • 0041371767 scopus 로고    scopus 로고
    • 3 "baconipyrones are proposed to be rearrangement products generated from a siphonariid precursor..." or "are generated as artifacts during the extraction."
    • 3 "baconipyrones are proposed to be rearrangement products generated from a siphonariid precursor..." or "are generated as artifacts during the extraction."
  • 7
    • 33845374455 scopus 로고
    • Black, K. A.; Vogel, P. J. Org. Chem. 1986, 51, 5341. Compound 1 has been synthesized in optically pure form ([α]D = +235.0) starting from (+)-2-cyano-7-oxabicyclo[2.2.1]hept-5-en-2-yl camphanate. In this preliminary account racemic 1 has been used.
    • (1986) J. Org. Chem. , vol.51 , pp. 5341
    • Black, K.A.1    Vogel, P.2
  • 8
    • 0033607764 scopus 로고    scopus 로고
    • For a review on the use of 7-oxanorbornenic derivatives (Diels-Alder adducts of furan) as synthetic intermediates, see: Arjona, O.; Cossy, J.; Plumet, J.; Vogel, P. Tetrahedron 1999, 55, 13521
    • (1999) Tetrahedron , vol.55 , pp. 13521
    • Arjona, O.1    Cossy, J.2    Plumet, J.3    Vogel, P.4
  • 9
    • 0000164611 scopus 로고
    • The referee suggests a possible improvement of the yield of this process by application of a procedure previously described: Warm, A.; Vogel, P. J. Org. Chem. 1986, 51, 5348. We thank the referee for this valuable suggestion, which will be tested soon.
    • (1986) J. Org. Chem. , vol.51 , pp. 5348
    • Warm, A.1    Vogel, P.2
  • 14
    • 0041872508 scopus 로고    scopus 로고
    • This transformation can be achieved without isolation of the intermediate vinyl sulfone 5. In this case the overall yield for the transformation of 4 into 6 is 59%
    • This transformation can be achieved without isolation of the intermediate vinyl sulfone 5. In this case the overall yield for the transformation of 4 into 6 is 59%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.