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Volumn 5, Issue 4, 2014, Pages 1555-1560

Predicting pathways for terpene formation from first principles-routes to known and new sesquiterpenes

Author keywords

[No Author keywords available]

Indexed keywords

ARTIFICIAL FORCES; CARBOCATIONS; SESQUITERPENES;

EID: 84897729937     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c3sc53293c     Document Type: Article
Times cited : (29)

References (62)
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    • (2006) J. Phys. Chem. A , vol.110 , pp. 8933-8941
    • Ohno, K.1    Maeda, S.2
  • 43
    • 0003754095 scopus 로고
    • in, ed. Ziesche and H. Eschrig, Akademie Verlag, Berlin, p. 11
    • J. P. Perdew, in Electronic Structure of Solids ′91, ed., P. Ziesche, and, H. Eschrig, Akademie Verlag, Berlin, 1991, p. 11
    • (1991) Electronic Structure of Solids ′91
    • Perdew, J.P.1
  • 50
    • 20644462075 scopus 로고
    • Diastereomers of D are also precursors to known sesquiterpenes
    • A. V. Z. Tkachev Organich. Khim. 1990 26 1706 1710
    • (1990) Organich. Khim. , vol.26 , pp. 1706-1710
    • Tkachev, A.V.Z.1
  • 54
    • 84897680732 scopus 로고    scopus 로고
    • Our calculations on africanene formation using B3LYP/6-31+G(d,p) agree with those described herein, unpublished results
    • Our calculations on africanene formation using B3LYP/6-31+G(d,p) agree with those described herein, P. G. Gutta and D. J. Tantillo, unpublished results
    • Gutta, P.G.1    Tantillo, D.J.2
  • 58
    • 0002738811 scopus 로고
    • The skeletons of Y and X are similar to those of known triquinanes, but have different arrangements of methyl groups The chemical shifts for T -derived sesquiterpenes could be readily predicted using quantum chemical methods so as to facilitate their identification in the future. For leading references, see
    • J. B. Hendrickson Tetrahedron 1959 7 82 89
    • (1959) Tetrahedron , vol.7 , pp. 82-89
    • Hendrickson, J.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.