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Volumn 52, Issue 15, 2011, Pages 1788-1790

Total synthesis of topsentolide B2

Author keywords

Asymmetric dihydroxylation; Ring closing metathesis (RCM); Roush allylation; Stereoselective synthesis; Topsentolides

Indexed keywords

CYTOTOXIC AGENT; OXYLIPIN; TOPSENTOLIDE B2; UNCLASSIFIED DRUG;

EID: 79952534615     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.02.014     Document Type: Article
Times cited : (5)

References (37)
  • 24
    • 0034698149 scopus 로고    scopus 로고
    • Compound 10 was prepared following literature procedure, see: F.A. Davis, H. Qi, and G. Sundarababu Tetrahedron 56 2000 5303 5310
    • (2000) Tetrahedron , vol.56 , pp. 5303-5310
    • Davis, F.A.1    Qi, H.2    Sundarababu, G.3
  • 27
    • 72849114062 scopus 로고    scopus 로고
    • Compound 11 was prepared following a similar literature procedure, see: C.R. Reddy, G. Dharmapuri, and N.N. Rao Org. Lett. 11 2009 5730 5733
    • (2009) Org. Lett. , vol.11 , pp. 5730-5733
    • Reddy, C.R.1    Dharmapuri, G.2    Rao, N.N.3
  • 28
    • 79952537355 scopus 로고    scopus 로고
    • Asymmetric dihydroxylation of 11 was similar to the synthesis of ent-11 as reported in the above reference
    • Asymmetric dihydroxylation of 11 was similar to the synthesis of ent-11 as reported in the above reference.
  • 29
    • 20444490799 scopus 로고    scopus 로고
    • For similar regio- and stereoselective asymmetric dihydroxylation of distant olefinic bond of a α,β,γ,δ-unsaturated esters see: Y. Zhang, and G.A. O'Doherty Tetrahedron 61 2005 6337 6351
    • (2005) Tetrahedron , vol.61 , pp. 6337-6351
    • Zhang, Y.1    O'Doherty, G.A.2
  • 33
    • 79952534446 scopus 로고    scopus 로고
    • +: 311.2222, found: 311.2225.
    • +: 311.2222, found: 311.2225.
  • 34
    • 79952533648 scopus 로고    scopus 로고
    • +: 427.2824, found: 427.2831.
    • +: 427.2824, found: 427.2831.
  • 35
    • 79952536767 scopus 로고    scopus 로고
    • For a similar low yielding RCM reaction in the synthesis of helicholactone using Grubbs-II catalyst see Ref. 4a
    • For a similar low yielding RCM reaction in the synthesis of helicholactone using Grubbs-II catalyst see Ref. 4a.
  • 36
    • 79952534640 scopus 로고    scopus 로고
    • 4 (in the synthesis of halicholactone) see Refs. 4a and 4d
    • 4 (in the synthesis of halicholactone) see Refs. 4a and 4d.
  • 37
    • 79952534758 scopus 로고    scopus 로고
    • +: 359.2356, found: 359.2350
    • +: 359.2356, found: 359.2350.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.