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Volumn 133, Issue 26, 2011, Pages 9952-9955

Total synthesis and absolute stereochemical assignment of kibdelone C

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL REACTIONS; ANTI-CANCER AGENTS; RING FRAGMENTS; TOTAL SYNTHESIS;

EID: 79959864466     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja203642n     Document Type: Article
Times cited : (79)

References (61)
  • 10
    • 84986397978 scopus 로고
    • For synthetic work on polycyclic xanthones, see the following. Lysolipin
    • For synthetic work on polycyclic xanthones, see the following. Lysolipin: Duthaler, R. O.; Wegmann, U. H. Helv. Chim. Acta 1984, 67, 1217-1211
    • (1984) Helv. Chim. Acta , vol.67 , pp. 1217-1211
    • Duthaler, R.O.1    Wegmann, U.H.2
  • 17
    • 44349084170 scopus 로고    scopus 로고
    • For a review on oxa -Michael reactions, see:;, For oxa -Michael reactions of 4-hydroxycyclohexenone, see:;; Angew. Chem., Int. Ed. 2006, 45, 307-309
    • For a review on oxa -Michael reactions, see: Nising, C. F.; Bräse, S. Chem. Soc. Rev. 2008, 37, 1218-1228 For oxa -Michael reactions of 4-hydroxycyclohexenone, see: Nising, C. F.; Ohnemüller, U. K.; Bräse, S. Angew. Chem., Int. Ed. 2006, 45, 307-309
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 1218-1228
    • Nising, C.F.1    Bräse, S.2    Nising, C.F.3    Ohnemüller, U.K.4    Bräse, S.5
  • 18
    • 26044481179 scopus 로고    scopus 로고
    • For xanthone synthesis through diaryl ether formation followed by intramolecular Friedel - Crafts annulations, see ref 3 and the following
    • For xanthone synthesis through diaryl ether formation followed by intramolecular Friedel - Crafts annulations, see ref 3 and the following: Sousa, M. E.; Pinto, M. M. M. Curr. Med. Chem. 2005, 12, 2447-2479
    • (2005) Curr. Med. Chem. , vol.12 , pp. 2447-2479
    • Sousa, M.E.1    Pinto, M.M.M.2
  • 24
    • 0035932604 scopus 로고    scopus 로고
    • Org. Lett. 2001, 3, 823-826.
    • (2001) Org. Lett. , vol.3 , pp. 823-826
  • 37
    • 79959908586 scopus 로고    scopus 로고
    • See Supporting Information for complete experimental details.
    • See Supporting Information for complete experimental details.
  • 42
    • 70349786460 scopus 로고    scopus 로고
    • For a review on Cu-catalyzed Ullmann coupling, see
    • For a review on Cu-catalyzed Ullmann coupling, see: Monnier, F.; Taillefer, M. Angew. Chem., Int. Ed. 2009, 48, 6954-6971
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6954-6971
    • Monnier, F.1    Taillefer, M.2
  • 43
    • 77949297216 scopus 로고    scopus 로고
    • For diaryl ether synthesis using picolinic acid/Cu(I), see
    • For diaryl ether synthesis using picolinic acid/Cu(I), see: Maiti, D.; Buchwald, S. L. J. Org. Chem. 2010, 75, 1791-1794
    • (2010) J. Org. Chem. , vol.75 , pp. 1791-1794
    • Maiti, D.1    Buchwald, S.L.2
  • 45
    • 33845282043 scopus 로고
    • For σ - π* interactions in osmylations, see
    • For σ - π* interactions in osmylations, see: Johnson, C. R.; Tait, B. D.; Cieplak, A. S. J. Am. Chem. Soc. 1987, 109, 5875-5876
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 5875-5876
    • Johnson, C.R.1    Tait, B.D.2    Cieplak, A.S.3
  • 50
    • 51649086416 scopus 로고    scopus 로고
    • For a recent review on cyanuric chloride, see: Tetrahedron 2006, 62, 9507-9522
    • Kangani, C. O.; Day, B. W. Org. Lett. 2008, 10, 2645-2648 For a recent review on cyanuric chloride, see: Blotny, G. Tetrahedron 2006, 62, 9507-9522
    • (2008) Org. Lett. , vol.10 , pp. 2645-2648
    • Kangani, C.O.1    Day, B.W.2    Blotny, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.