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Volumn 107, Issue 9, 2007, Pages 3744-3779

Determination of relative configuration in organic compounds by NMR spectroscopy and computational methods

Author keywords

[No Author keywords available]

Indexed keywords

COMPUTATIONAL METHODS; NUCLEAR MAGNETIC RESONANCE; QUANTUM THEORY; STEREOCHEMISTRY;

EID: 35148813913     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr030733c     Document Type: Review
Times cited : (509)

References (195)
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    • Gomez-Paloma, L.; Bifulco, G.; Bassarello, C.; Cimino, P. In Seminars in Organic Synthesis, Summer School "A. Corbella", 26th, Gargnano, Italy, June 18-22, 2001; Società Chimica Italiana: Rome, Italy, 2001; pp 145-171.
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    • HC see: Marquez, B. L.; Gerwick, W. H.; Williamson, R. T. Magn. Reson. Chem. 2001, 39, 499.
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    • Ciminiello, P.; Dell'Aversano, C.; Fattorusso, E.; Forino, M.; Magno, &; Di Rosa, M.; lanaro, A.; Poletti, R. J. Am. Chem. Soc. 2002, 124, 13114.
  • 88
    • 0033619850 scopus 로고    scopus 로고
    • The UDB acronym was purposefully created by the authors of this review and used throughout the paper
    • (b) Lee, J.; Kobayashi, Y.; Tezuka, K.; Kishi, Y. Org. Lett. 1999, 1, 2181. The UDB acronym was purposefully created by the authors of this review and used throughout the paper.
    • (1999) Org. Lett , vol.1 , pp. 2181
    • Lee, J.1    Kobayashi, Y.2    Tezuka, K.3    Kishi, Y.4
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    • For a review on Palitoxin, see
    • For a review on Palitoxin, see: Kishi, Y. Tetrahedron 2002, 58, 6239.
    • (2002) Tetrahedron , vol.58 , pp. 6239
    • Kishi, Y.1
  • 90
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    • For each nucleus (proton or carbon) of each diastereoisomer, the differences of the experimentally measured cs from the computed mean values were plotted as histograms
    • For each nucleus (proton or carbon) of each diastereoisomer, the differences of the experimentally measured cs from the computed mean values were plotted as histograms.
  • 91
    • 35148835947 scopus 로고    scopus 로고
    • For each nucleus (proton or carbon) of each diastereoisomer, the mean value of the experimentally measured es was computed
    • For each nucleus (proton or carbon) of each diastereoisomer, the mean value of the experimentally measured es was computed.
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    • CambridgeSoft
    • CambridgeSoft.
  • 97
    • 35148855546 scopus 로고    scopus 로고
    • The absolute configurations of the stereocenters were assigned by comparing the optical rotation of the synthesized fragments and the degradation products (for C21-C38 segment) or synthesizing the Mosher esters of both synthesized or degradated products C5-C10, C41-C43, C14-C15, and C18-C19 segments, See ref 95d
    • The absolute configurations of the stereocenters were assigned by comparing the optical rotation of the synthesized fragments and the degradation products (for C21-C38 segment) or synthesizing the Mosher esters of both synthesized or degradated products (C5-C10, C41-C43, C14-C15, and C18-C19 segments). See ref 95d.
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    • (a) http://www.nmrshiftdb.org.
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    • Lipkowitz, K. B, Boyd, D. B, Eds, VCH: New York, Chapter 5, pp
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    • Chesnut, D.B.1
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    • MACROMODEL 4.5, Department of Chemistry, Columbia University, New York, NY.
    • MACROMODEL 4.5, Department of Chemistry, Columbia University, New York, NY.
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    • The reader interested in this specific area may consult recent reviews on the subject: (a) Gschwind, R. M. Angew. Chem. Int. Ed. 2005, 44, 4666.
    • The reader interested in this specific area may consult recent reviews on the subject: (a) Gschwind, R. M. Angew. Chem. Int. Ed. 2005, 44, 4666.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.