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Volumn 14, Issue 4, 2012, Pages 1054-1057

Stereoselective synthesis of cis-2,5-disubstituted THFs: Application to adjacent bis-THF cores of annonaceous acetogenins

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; FURAN DERIVATIVE; TETRAHYDROFURAN;

EID: 84857207914     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol203425p     Document Type: Article
Times cited : (20)

References (34)
  • 17
    • 84857213947 scopus 로고    scopus 로고
    • Reference 7.
    • Reference 7.
  • 19
    • 67149140506 scopus 로고    scopus 로고
    • For a recent review for total synthesis of Annonaceous acetogenins, see
    • For a recent review for total synthesis of Annonaceous acetogenins, see: Li, N.; Shi, Z.; Tang, Y.; Chen, J.; Li, X. Beilstein J. Org. Chem. 2008, 4, 48
    • (2008) Beilstein J. Org. Chem. , vol.4 , pp. 48
    • Li, N.1    Shi, Z.2    Tang, Y.3    Chen, J.4    Li, X.5
  • 28
    • 0033516435 scopus 로고    scopus 로고
    • Diol 8 was prepared from commercially available trans -1,5,9-decatriene in one step (57% yield).
    • Diol 8 was prepared from commercially available trans -1,5,9-decatriene in one step (57% yield). Tian, S.-K.; Wang, Z.-M.; Jiang, J.-K.; Shi, M. Tetrahedron: Asymmetry 1999, 10, 2551
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2551
    • Tian, S.-K.1    Wang, Z.-M.2    Jiang, J.-K.3    Shi, M.4
  • 29
    • 21944442123 scopus 로고    scopus 로고
    • The iodocyclization of ent - 8 with iodine gave trans / threo / trans bis-THF product as a major isomer with a 7:1 selectivity
    • The iodocyclization of ent-8 with iodine gave trans / threo / trans bis-THF product as a major isomer with a 7:1 selectivity: Lee, S.; Lee, Y.-S.; Park, G.; Choi, S.; Yoon, S.-H. Bull. Korean Chem. Soc. 1998, 19, 115
    • (1998) Bull. Korean Chem. Soc. , vol.19 , pp. 115
    • Lee, S.1    Lee, Y.-S.2    Park, G.3    Choi, S.4    Yoon, S.-H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.