메뉴 건너뛰기




Volumn 9, Issue 5, 2014, Pages 1274-1277

Diels-alder/oxidative aromatization approach towards the all-carbon def tricyclic skeleton of daphenylline

Author keywords

alkaloids; aromatization; daphenylline; Diels Alder; natural products

Indexed keywords

ALKALOIDS; CARBON; CONDENSATION REACTIONS; METABOLITES; MUSCULOSKELETAL SYSTEM; NITROGEN COMPOUNDS; SCAFFOLDS; SYNTHESIS (CHEMICAL);

EID: 84899460808     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201400002     Document Type: Article
Times cited : (27)

References (64)
  • 1
    • 84899438744 scopus 로고    scopus 로고
    • For selected recent isolations of Daphniphyllum alkaloids, see
    • For selected recent isolations of Daphniphyllum alkaloids, see
  • 11
    • 33646673897 scopus 로고    scopus 로고
    • Editorial Committee of the Administration Bureau of Traditional Chinese Medicine in Chinese Materia. 4, Shanghai Science&Technology Press, Shanghai
    • Editorial Committee of the Administration Bureau of Traditional Chinese Medicine in Chinese Materia. Zhonghua Bencao, Vol. 4, Shanghai Science&Technology Press, Shanghai, 1998, pp. 865-867.
    • (1998) Zhonghua Bencao , pp. 865-867
  • 12
    • 84899436691 scopus 로고    scopus 로고
    • For completed total syntheses of Daphniphyllum alkaloids, see
    • For completed total syntheses of Daphniphyllum alkaloids, see
  • 21
    • 84867438092 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 11703-11707
    • (2011) Angew. Chem. , vol.123 , pp. 11703-11707
  • 24
    • 84899455323 scopus 로고    scopus 로고
    • For synthetic strategies for skeletons of Daphniphyllum alakloids, see
    • For synthetic strategies for skeletons of Daphniphyllum alakloids, see
  • 39
    • 84899465296 scopus 로고    scopus 로고
    • For synthetic strategies for construction of the ring system of daphenylline developed by our reserach group, see
    • For synthetic strategies for construction of the ring system of daphenylline developed by our reserach group, see
  • 40
    • 84899453805 scopus 로고    scopus 로고
    • Ph. D. thesis, Lanzhou University
    • J. Zheng, Ph. D. thesis, Lanzhou University, 2010
    • (2010)
    • Zheng, J.1
  • 44
    • 84899462290 scopus 로고    scopus 로고
    • With respect to the structure of daphenylline, in our viewpoint (Ref. 5c), it does not belong to the known structure types classified by J. Kobayashi (Ref. 1h). However, Li and co-workers hold a different view that daphenylline is a calyciphylline A-type alkaloid (Ref. 3i). Finally, according to the most recent literature, Xu and co-workers point supported our view (Ref. 1i)
    • With respect to the structure of daphenylline, in our viewpoint (Ref. 5c), it does not belong to the known structure types classified by J. Kobayashi (Ref. 1h). However, Li and co-workers hold a different view that daphenylline is a calyciphylline A-type alkaloid (Ref. 3i). Finally, according to the most recent literature, Xu and co-workers point supported our view (Ref. 1i).
  • 47
    • 0024573545 scopus 로고
    • For selected reports on the Swern oxidation of diols into dialdehydes, see
    • For selected reports on the Swern oxidation of diols into dialdehydes, see, M. Sodeoka, Y. Ogawa, T, Mase, M. Shibasaki, Chem. Pharm. Bull. 1989, 37, 586-598.
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 586-598
    • Sodeoka, M.1    Ogawa, Y.2    Mase, T.3    Shibasaki, M.4
  • 48
    • 84899440695 scopus 로고    scopus 로고
    • For intramolecular aldol condensations of dialdehyde, see
    • For intramolecular aldol condensations of dialdehyde, see
  • 51
    • 84899425259 scopus 로고    scopus 로고
    • For recent reviews on Diels-Alder reactions, see
    • For recent reviews on Diels-Alder reactions, see
  • 53
    • 84880100773 scopus 로고    scopus 로고
    • For triple bond as dienophile in Diels-Alder cycloaddition, see
    • X. Jiang, R. Wang, Chem. Rev. 2013, 113, 5515-5546. For triple bond as dienophile in Diels-Alder cycloaddition, see
    • (2013) Chem. Rev. , vol.113 , pp. 5515-5546
    • Jiang, X.1    Wang, R.2
  • 56
    • 76649109010 scopus 로고    scopus 로고
    • Angew. Chem. 2009, 121, 8204-8206
    • (2009) Angew. Chem. , vol.121 , pp. 8204-8206
  • 59
    • 84899449173 scopus 로고    scopus 로고
    • For oxidative aromatization of 1,3-dienes with DDQ, see
    • For oxidative aromatization of 1,3-dienes with DDQ, see
  • 64
    • 0842277228 scopus 로고    scopus 로고
    • 2 as solvent, the desired reaction occurred with good yields at 0C
    • 2 as solvent, the desired reaction occurred with good yields at 0C.
    • (2003) Angew. Chem. , vol.115 , pp. 2901-2903


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.