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Volumn 61, Issue 8, 1996, Pages 2738-2742

Development of molecular mechanics torsion parameters for α,β-cyclopropyl ketones and conformational analysis of bicyclo[m.1.0]alkan-2-ones

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EID: 0343900887     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951752s     Document Type: Article
Times cited : (6)

References (77)
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    • (b) Barton, D. H. R. Experientia 1950, 6, 316. Or see: Top. Stereochem. 1971,6, 1-10.
    • (1950) Experientia , vol.6 , pp. 316
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  • 5
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    • (b) Barton, D. H. R. Experientia 1950, 6, 316. Or see: Top. Stereochem. 1971,6, 1-10.
    • (1971) Top. Stereochem. , vol.6 , pp. 1-10
  • 13
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    • d. l. Mare, P. B. D., Klyne, W., Eds.; Butterworths: Washington
    • (b) Sicher, J. In Progress in Stereochemistry; d. l. Mare, P. B. D., Klyne, W., Eds.; Butterworths: Washington, 1962; Vol. 3; pp 202-263.
    • (1962) Progress in Stereochemistry , vol.3 , pp. 202-263
    • Sicher, J.1
  • 24
    • 85050276614 scopus 로고
    • Allinger, N. L., Eliel, E. L., Eds.; Wiley Interscience: New York
    • (m) Dale, J. In Topics in Stereochemistry; Allinger, N. L., Eliel, E. L., Eds.; Wiley Interscience: New York, 1976; Vol. 9; pp 199-270.
    • (1976) Topics in Stereochemistry , vol.9 , pp. 199-270
    • Dale, J.1
  • 37
    • 0002015005 scopus 로고
    • Lipkowitz, K. B., Boyd, D. B., Eds.; VCH Publishers, Inc.: New York
    • (f) Leach, A. R. In Reviews in Computational Chemistry; Lipkowitz, K. B., Boyd, D. B., Eds.; VCH Publishers, Inc.: New York, 1991: Vol. 2, pp 1-55.
    • (1991) Reviews in Computational Chemistry , vol.2 , pp. 1-55
    • Leach, A.R.1
  • 42
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    • Mash, E. A.; Kaczynski, M. A.; Dolata, D. P. Tetrahedron Lett. 1990, 31, 4065-4568. The identities of the major and minor diastereomers 4a and 4b were unknown at the time of this communication.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 4065-4568
    • Mash, E.A.1    Kaczynski, M.A.2    Dolata, D.P.3
  • 43
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    • and references cited therein
    • (a) Kamernitzky, A. V.; Akhrem, A. A. Tetrahedron 1962, 18, 705-750 and references cited therein,
    • (1962) Tetrahedron , vol.18 , pp. 705-750
    • Kamernitzky, A.V.1    Akhrem, A.A.2
  • 48
    • 0342595174 scopus 로고
    • Columbia University, New York
    • BATCHMIN, 4.0; Columbia University, New York, 1993.
    • (1993) BATCHMIN, 4.0
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    • Wavefunction, Inc., Irvine, CA
    • Spartan, 4.0; Wavefunction, Inc., Irvine, CA, 1990.
    • (1990) Spartan, 4.0
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    • note
    • The numbering scheme refers to the IUPAC numbering of the bicyclo[m.1.0]alkan-2-ones; the carbonyl is C(2), the α-cyclopropyl carbon is C(1), and the α-hydrogen is H(1).
  • 73
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    • See ref 1, p 654 and accompanying discussion
    • See ref 1, p 654 and accompanying discussion.
  • 74
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    • Ph.D. Dissertation, The University of Arizona
    • Matthew T. Stahl, Ph.D. Dissertation, The University of Arizona, 1995.
    • (1995)
    • Stahl, M.T.1
  • 76
    • 0025049742 scopus 로고
    • Vedejs' concept of local conformational control has previously been advanced as applicable to medium- and large-ring cyclopropyl ketones; see: Dolata, D. P.; Spina, D. R. Tetrahedron Lett. 1990, 31, 6811-6814.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 6811-6814
    • Dolata, D.P.1    Spina, D.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.