메뉴 건너뛰기




Volumn 55, Issue 28, 2014, Pages 3817-3819

Studies in symmetry-driven synthesis of ryanodol: Application of nucleophilic alkynylation for regio- and stereoselective desymmetrization

Author keywords

Desymmetrization; Fused ring systems; Magnesium ate complex; Terpenoid

Indexed keywords

RYANODINE; RYANODOL; UNCLASSIFIED DRUG;

EID: 84902537518     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.05.075     Document Type: Article
Times cited : (5)

References (29)
  • 8
    • 58149514666 scopus 로고    scopus 로고
    • For synthetic studies of ryanodol from our laboratory, see: (a)
    • For synthetic studies of ryanodol from our laboratory, see: (a) K. Hagiwara, M. Himuro, M. Hirama, and M. Inoue Tetrahedron Lett. 50 2009 1035
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1035
    • Hagiwara, K.1    Himuro, M.2    Hirama, M.3    Inoue, M.4
  • 10
    • 84874644360 scopus 로고    scopus 로고
    • Synthesis of enantiopure intermediates, see
    • Synthesis of enantiopure intermediates, see M. Iwatsu, D. Urabe, and M. Inoue Heterocycles 82 2010 491
    • (2010) Heterocycles , vol.82 , pp. 491
    • Iwatsu, M.1    Urabe, D.2    Inoue, M.3
  • 13
    • 0043236240 scopus 로고    scopus 로고
    • Symmetry-driven synthesis of the natural products from our laboratory. Merrilactone A: (a)
    • Symmetry-driven synthesis of the natural products from our laboratory. Merrilactone A: (a) M. Inoue, T. Sato, and M. Hirama J. Am. Chem. Soc. 125 2003 10772
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10772
    • Inoue, M.1    Sato, T.2    Hirama, M.3
  • 18
    • 0028799792 scopus 로고
    • For reviews on desymmetrization in the context of natural product synthesis, see: (a)
    • For reviews on desymmetrization in the context of natural product synthesis, see: (a) S.R. Magnuson Tetrahedron 51 1995 2167
    • (1995) Tetrahedron , vol.51 , pp. 2167
    • Magnuson, S.R.1
  • 21
    • 0038190214 scopus 로고
    • Upon treatment with a bulky and anionic nucleophile, the 1,2-diketone moiety of 2 was prone to undergo reduction into the corresponding α-hydroxy ketone, presumably through the single electron transfer (SET) mechanism. The SET process appeared to be involved in other decomposition pathways. For related examples, see: (a)
    • Upon treatment with a bulky and anionic nucleophile, the 1,2-diketone moiety of 2 was prone to undergo reduction into the corresponding α-hydroxy ketone, presumably through the single electron transfer (SET) mechanism. The SET process appeared to be involved in other decomposition pathways. For related examples, see: (a) G.B. Bennett, W.J. Houlihan, and R.B. Mason J. Organomet. Chem. 99 1975 185
    • (1975) J. Organomet. Chem. , vol.99 , pp. 185
    • Bennett, G.B.1    Houlihan, W.J.2    Mason, R.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.