메뉴 건너뛰기




Volumn 15, Issue 24, 2009, Pages 5979-5997

The laulimalide family: Total synthesis and biological evaluation of neolaulimalide, isolaulimalide, laulimalide and a nonnatural analogue

Author keywords

Acyl migration; Antitumor agents; Natural products; Olefination; Total synthesis

Indexed keywords

ACYL MIGRATION; ANTITUMOR AGENTS; NATURAL PRODUCTS; OLEFINATION; TOTAL SYNTHESIS;

EID: 66349099585     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200802605     Document Type: Article
Times cited : (55)

References (64)
  • 5
    • 34548095481 scopus 로고    scopus 로고
    • T. A. Johnson, K. Tenney, R. H. Cichewicz, B. I. Morinaka, K. N. White, T. Amagata, B. Subramanian, J. Media, S. L. Mooberry, F. A. Valeriote, P. Crews, J. Med. Chem. 2007, 50, 3795-3803.
    • T. A. Johnson, K. Tenney, R. H. Cichewicz, B. I. Morinaka, K. N. White, T. Amagata, B. Subramanian, J. Media, S. L. Mooberry, F. A. Valeriote, P. Crews, J. Med. Chem. 2007, 50, 3795-3803.
  • 13
    • 34548095481 scopus 로고    scopus 로고
    • T. A. Johnson, K. Tenney, R. H. Cichewicz, B. I. Morinaka, K. N. White, T. Amagata, B. Subramanian, J. Media, S. L. Mooberry, F. A. Valeriote, P. Crews, J. Med. Chem. 2007, 50, 3795-3803.
    • T. A. Johnson, K. Tenney, R. H. Cichewicz, B. I. Morinaka, K. N. White, T. Amagata, B. Subramanian, J. Media, S. L. Mooberry, F. A. Valeriote, P. Crews, J. Med. Chem. 2007, 50, 3795-3803.
  • 14
    • 0034623543 scopus 로고    scopus 로고
    • Total synthesis of 1: a A. K. Ghosh, Y. Wang, J. Am. Chem. Soc. 2000, 122, 11027-11028.
    • Total synthesis of 1: a) A. K. Ghosh, Y. Wang, J. Am. Chem. Soc. 2000, 122, 11027-11028.
  • 16
    • 66349123380 scopus 로고    scopus 로고
    • J. Mulzer, E. Öhler Angew. Chem. 2001, 113, 3961-3964; Angew. Chem. Int. Ed. 2001, 40, 3842-3846; Angew. Chem. Int. Ed. 2001, 40, 3842-3846.
    • J. Mulzer, E. Öhler Angew. Chem. 2001, 113, 3961-3964; Angew. Chem. Int. Ed. 2001, 40, 3842-3846; Angew. Chem. Int. Ed. 2001, 40, 3842-3846.
  • 25
    • 66349116544 scopus 로고    scopus 로고
    • J. Uenishi, M. Ohmi, Angew. Chem. 2005, 117, 2816-2820; Angew. Chem. Int. Ed. 2005, 44, 2756-2760.
    • J. Uenishi, M. Ohmi, Angew. Chem. 2005, 117, 2816-2820; Angew. Chem. Int. Ed. 2005, 44, 2756-2760.
  • 26
    • 0141508044 scopus 로고    scopus 로고
    • For a review, see: m
    • For a review, see: m) J. Mulzer, E. Öhler, Chem. Rev. 2003, 80, 3753-3786.
    • (2003) Chem. Rev , vol.80 , pp. 3753-3786
    • Mulzer, J.1    Öhler, E.2
  • 27
    • 0345255654 scopus 로고    scopus 로고
    • Synthesis of analogues of 1: a P. A. Wender, S. G. Hegde, R. D. Hubbard, L. Zhang, S. L. Mooberry, Org. Lett. 2003, 5, 3507-3509.
    • Synthesis of analogues of 1: a) P. A. Wender, S. G. Hegde, R. D. Hubbard, L. Zhang, S. L. Mooberry, Org. Lett. 2003, 5, 3507-3509.
  • 40
    • 0032580376 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) R. H. Grubbs, S. Chang, Tetrahedron 1998, 54, 4413-4450.
    • (1998) Tetrahedron , vol.54 , pp. 4413-4450
    • Grubbs, R.H.1    Chang, S.2
  • 42
    • 66349118999 scopus 로고    scopus 로고
    • A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043.
    • A. Fürstner, Angew. Chem. 2000, 112, 3140-3172; Angew. Chem. Int. Ed. 2000, 39, 3012-3043.
  • 57
    • 0000018360 scopus 로고    scopus 로고
    • J. H. Wengrovius, J. Sancho, R. R. Schrock, J. Am. Chem. Soc. 1981, 103, 3932-3934. For a review, see: R. R. Schrock, Chem. Rev. 2002, 79, 145-179.
    • J. H. Wengrovius, J. Sancho, R. R. Schrock, J. Am. Chem. Soc. 1981, 103, 3932-3934. For a review, see: R. R. Schrock, Chem. Rev. 2002, 79, 145-179.
  • 58
    • 66349091732 scopus 로고    scopus 로고
    • We tried different solvents (PhH, PhMe) combined with variation of the temperature (RT to reflux) for RCAM
    • We tried different solvents (PhH, PhMe) combined with variation of the temperature (RT to reflux) for RCAM.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.