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Volumn 58, Issue 2-3, 2003, Pages 231-236

Structural Investigation of a Configurationally Stable Seven-Membered Bridged Biaryl of Relevance for Atroposelective Biaryl Syntheses

Author keywords

Bridged Biaryls; Crystal Structure; Density Functional Theory Calculations

Indexed keywords

CALCULATIONS; DENSITY FUNCTIONAL THEORY; DIHEDRAL ANGLE; ESTERS; ETHERS; STEREOCHEMISTRY; X RAY POWDER DIFFRACTION;

EID: 0038135329     PISSN: 09320776     EISSN: None     Source Type: Journal    
DOI: 10.1515/znb-2003-2-305     Document Type: Article
Times cited : (2)

References (32)
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    • For a selection of novel methods for the stereoselective construction of biaryl axis, see: a) J. Hassan, M. Sevignon, C. Gozzi, E. Schülz, M. Lemaire, Chem. Rev. 102, 1359-1469 (2002);
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    • For the use of seven-membered bridged biaryls in the syntheses of the nerve growth stimulating natural product mastigophorene A see
    • For the use of seven-membered bridged biaryls in the syntheses of the nerve growth stimulating natural product mastigophorene A see: G. Bringmann, J. Hinrichs, T. Pabst, P. Henschel, K. Peters, E. -M. Peters, Synthesis 155-167 (2001).
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    • Bringmann, G.1    Hinrichs, J.2    Pabst, T.3    Henschel, P.4    Peters, K.5    Peters, E.-M.6
  • 17
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    • For the synthesis and ring opening of other related seven-membered bridged biaryls, see: a)
    • For the synthesis and ring opening of other related seven-membered bridged biaryls, see: a) G. Bringmann, J. Hinrichs, P. Henschel, K. Peters, E. -M. Peters, Synlett 1822-1824 (2000);
    • (2000) Synlett , pp. 1822-1824
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  • 24
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    • For atroposelective syntheses of axially chiral natural biaryl products via cyclic ethers, see
    • For atroposelective syntheses of axially chiral natural biaryl products via cyclic ethers, see: G. Bringmann, J. R. Jansen, Heterocycles 28, 137-142 (1989).
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    • Bringmann, G.1    Jansen, J.R.2
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    • SYBYL: Tripos Associates


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.