메뉴 건너뛰기




Volumn 52, Issue 38, 2013, Pages 9970-9975

Rapid access to dibenzohelicenes and their functionalized derivatives

Author keywords

alkynes; aromaticity; asymmetric synthesis; chirality; helical structures

Indexed keywords

ALKYNES; AROMATICITIES; ASYMMETRIC SYNTHESIS; CYCLOISOMERIZATIONS; DESILYLATION; FUNCTIONALIZED; HELICAL STRUCTURES; SUZUKI-MIYAURA COUPLING;

EID: 84884219334     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201301739     Document Type: Article
Times cited : (122)

References (69)
  • 6
    • 79551538813 scopus 로고    scopus 로고
    • (Eds.: J. S. Siegel, Y. Tobe), Thieme, Stuttgart
    • I. G. Stará, I. Starý, in Science of Synthesis, Vol. 45b (Eds.:, J. S. Siegel, Y. Tobe,), Thieme, Stuttgart, 2010, pp. 885-953
    • (2010) Science of Synthesis, Vol. 45b , pp. 885-953
    • Stará, I.G.1    Starý, I.2
  • 8
    • 79960322536 scopus 로고    scopus 로고
    • (Ed.: H. Dodziuk), Wiley-VCH, Weinheim
    • I. Starý, I. G. Stará, in Strained Hydrocarbons (Ed.:, H. Dodziuk,), Wiley-VCH, Weinheim, 2009, pp. 166-176
    • (2009) Strained Hydrocarbons , pp. 166-176
    • Starý, I.1    Stará, I.G.2
  • 9
    • 84891318563 scopus 로고    scopus 로고
    • (Eds.: T. J. J. Müller, U. H. F. Bunz), Wiley-VCH, Weinheim
    • A. Rajca, M. Miyasaka, in Functional Organic Materials (Eds.:, T. J. J. Müller, U. H. F. Bunz,), Wiley-VCH, Weinheim, 2007, pp. 547-581
    • (2007) Functional Organic Materials , pp. 547-581
    • Rajca, A.1    Miyasaka, M.2
  • 12
  • 15
  • 16
  • 31
    • 84255177872 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 12582-12585
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 12582-12585
  • 35
    • 57149089914 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 9708-9710; in enantioselective propargylation of aldehydes
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9708-9710
  • 36
  • 40
    • 51049114227 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 3188-3191
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3188-3191
  • 44
    • 0037009020 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3227-3230.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3227-3230
  • 50
    • 14644440886 scopus 로고    scopus 로고
    • Although the Suzuki-Miyaura reaction with the arylboronic acid pinacol ester 9 is possible, the respective free arylboronic acid is more practical to prepare and purify owing to its better stability (see the Supporting Information). For the synthesis of 9, see:, B. Felber, F. Diederich, Helv. Chim. Acta 2005, 88, 120-153.
    • (2005) Helv. Chim. Acta , vol.88 , pp. 120-153
    • Felber, B.1    Diederich, F.2
  • 52
    • 61349084243 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1810-1813.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1810-1813
  • 53
    • 84884230733 scopus 로고    scopus 로고
    • CCDC 920132 (rac- 2) and 920131 (rac- 25) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 920132 (rac- 2) and 920131 (rac- 25) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
  • 64
  • 69
    • 84861871496 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 5857-5861.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5857-5861


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.