메뉴 건너뛰기




Volumn 14, Issue 3, 2008, Pages 829-837

Highly efficient total synthesis of the marine natural products (+)-avarone, (+)-avarol, (-)-neoavarone, (-)-neoavarol and (+)-aureol

Author keywords

Biomimetic synthesis; Natural products; Quinones; Rearrangement; Total synthesis

Indexed keywords

BIOMIMETIC SYNTHESIS; CYTOTOXIC POTENCY; NATURAL PRODUCTS;

EID: 38849168232     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701386     Document Type: Article
Times cited : (52)

References (55)
  • 1
    • 77957087867 scopus 로고    scopus 로고
    • For recent excellent reviews on the clerodane diterpenoids and related compounds including marine natural products; see: a) R. J. Capon, in Studies in Natural Products Chemistry, 15 Ed, Attaur-Rahman, Elsevier, Amsterdam, 1995, p. 289-326;
    • For recent excellent reviews on the clerodane diterpenoids and related compounds including marine natural products; see: a) R. J. Capon, in Studies in Natural Products Chemistry, Vol. 15 (Ed.: Attaur-Rahman), Elsevier, Amsterdam, 1995, p. 289-326;
  • 5
    • 38849174190 scopus 로고    scopus 로고
    • S. De Rosa, in Natural Products in the New Millennium: Prospects and Industrial Application (Eds. : A. P. Rauter, F. B. Palma, J. Justino, M. E. Araújo, S. P. Santos), Kluwer, Dordrecht, 2002, p. 441-461;
    • e) S. De Rosa, in Natural Products in the New Millennium: Prospects and Industrial Application (Eds. : A. P. Rauter, F. B. Palma, J. Justino, M. E. Araújo, S. P. Santos), Kluwer, Dordrecht, 2002, p. 441-461;
  • 26
    • 38849195991 scopus 로고    scopus 로고
    • A. E. Wright, S. S. Cross, N. S. Burres, F. Koehn Harbor Branch Oceanographics Institution, Inc, USA, PCT WO 9112250A1, August 22, 1991
    • A. E. Wright, S. S. Cross, N. S. Burres, F. Koehn (Harbor Branch Oceanographics Institution, Inc., USA), PCT WO 9112250A1, August 22, 1991.
  • 31
    • 0033581581 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 3089-3091;
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 3089-3091
  • 39
    • 38849145481 scopus 로고    scopus 로고
    • This type of reductive alkylation, originally explored by Stork et al
    • This type of reductive alkylation, originally explored by Stork et al.
  • 40
    • 0001632979 scopus 로고    scopus 로고
    • in the 1960s (a representative work; see: G. Stork, P. Rosen, N. Goldman, R. V. Coombs, J. Tsuji, J. Am. Chem. Soc. 1965, 87, 275-286), has been widely used as a critical step in the total synthesis of marine sesquiterpenoidal quinones and hydroquinones. For recent examples; see:
    • in the 1960s (a representative work; see: G. Stork, P. Rosen, N. Goldman, R. V. Coombs, J. Tsuji, J. Am. Chem. Soc. 1965, 87, 275-286), has been widely used as a critical step in the total synthesis of marine sesquiterpenoidal quinones and hydroquinones. For recent examples; see:
  • 45
    • 38849132467 scopus 로고    scopus 로고
    • [15]
    • [15]
  • 46
    • 0001879144 scopus 로고    scopus 로고
    • P. A. Bartlett, W.S. Johnson, Tetrahedron Lett. 1970, 11, 4459-nnn;
    • a) P. A. Bartlett, W.S. Johnson, Tetrahedron Lett. 1970, 11, 4459-nnn;
  • 52
    • 0001328194 scopus 로고    scopus 로고
    • 4 has been widely used for the conversion of sesquiterpenoidal quinones to the corresponding hydroquinones. For examples, see: a N. Harada, T. Sugioka, Y. Ando, H. Uda, T. Kuriki, J. Am. Chem. Soc. 1988, 110, 8483-8487;
    • 4 has been widely used for the conversion of sesquiterpenoidal quinones to the corresponding hydroquinones. For examples, see: a) N. Harada, T. Sugioka, Y. Ando, H. Uda, T. Kuriki, J. Am. Chem. Soc. 1988, 110, 8483-8487;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.