메뉴 건너뛰기




Volumn 18, Issue 10, 2012, Pages 2948-2960

Total synthesis of laulimalide: Synthesis of the northern and southern fragments

Author keywords

aldol reaction; asymmetric synthesis; chemoselectivity; macrocycles; total synthesis

Indexed keywords

ALDOL REACTIONS; ASYMMETRIC SYNTHESIS; CHEMO-SELECTIVITY; MACROCYCLES; TOTAL SYNTHESIS;

EID: 84857578082     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201102898     Document Type: Article
Times cited : (49)

References (116)
  • 42
    • 4444341915 scopus 로고    scopus 로고
    • a similar stereospecific palladium-catalyzed cyclization was reported by Lee and Hansen.
    • a similar stereospecific palladium-catalyzed cyclization was reported by Lee and Hansen:, E. C. Hansen, D. Lee, Tetrahedron Lett. 2004, 45, 7151.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7151
    • Hansen, E.C.1    Lee, D.2
  • 65
  • 71
    • 0012677208 scopus 로고    scopus 로고
    • references therein.
    • H. Kim, C. Lee, Org. Lett. 2002, 4, 4369, and references therein.
    • (2002) Org. Lett. , vol.4 , pp. 4369
    • Kim, H.1    Lee, C.2
  • 72
    • 0001793020 scopus 로고
    • in (Eds.: L.S. Hegedus, E. W. Abel, F. G. A. Stone, G. Wilkinson), Elsevier Science, New York, ; for early examples, see
    • J. M. Takacs, in Comprehensive Organometallic Chemistry II, Vol. 12 (Eds.:, L.S. Hegedus, E. W. Abel, F. G. A. Stone, G. Wilkinson,), Elsevier Science, New York, 1995, pp. 39-58; for early examples, see
    • (1995) Comprehensive Organometallic Chemistry II, Vol. 12 , pp. 39-58
    • Takacs, J.M.1
  • 88
    • 0012132823 scopus 로고    scopus 로고
    • in (Eds.: R. A. Sheldon, H. Bekkum), Wiley-VCH, Weinheim, p. .
    • T. Tatsumi, in Beckmann Rearrangement (Eds.:, R. A. Sheldon, H. Bekkum,), Wiley-VCH, Weinheim, 2001, p. 185.
    • (2001) Beckmann Rearrangement , pp. 185
    • Tatsumi, T.1
  • 91
    • 0142109730 scopus 로고    scopus 로고
    • For studies on the reactivity of acyl pyrroles, see
    • For studies on the reactivity of acyl pyrroles, see:, D. A. Evans, G. Borg, K. Scheidt, Angew. Chem. 2002, 114, 3320
    • (2002) Angew. Chem. , vol.114 , pp. 3320
    • Evans, D.A.1    Borg, G.2    Scheidt, K.3
  • 103
  • 111
    • 10044220689 scopus 로고    scopus 로고
    • for information on the mechanism of alkyne to vinylidene transformations, see.
    • for information on the mechanism of alkyne to vinylidene transformations, see:, Y. Wakatsuki, J. Organomet. Chem. 2004, 689, 4092.
    • (2004) J. Organomet. Chem. , vol.689 , pp. 4092
    • Wakatsuki, Y.1
  • 115
    • 12344298977 scopus 로고
    • I-catalyzed dimerization of terminal alkynes, see.
    • I-catalyzed dimerization of terminal alkynes, see:, H. J. Schmitt, H. Singer, J. Organomet. Chem. 1978, 153, 165.
    • (1978) J. Organomet. Chem. , vol.153 , pp. 165
    • Schmitt, H.J.1    Singer, H.2
  • 116
    • 0002313620 scopus 로고    scopus 로고
    • For the preparation and use of these types of stannane, see.
    • For the preparation and use of these types of stannane, see:, J. A. Marshall, Chem. Rev. 1996, 96, 31.
    • (1996) Chem. Rev. , vol.96 , pp. 31
    • Marshall, J.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.