메뉴 건너뛰기




Volumn 72, Issue 24, 2007, Pages 9264-9277

Pseudohelical and helical primary structures of 1,2-spiroannelated four- and five-membered rings: Syntheses and chiroptical properties

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; DENSITY FUNCTIONAL THEORY; OPTICAL ROTATION; SYNTHESIS (CHEMICAL);

EID: 36649011765     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7017558     Document Type: Article
Times cited : (17)

References (100)
  • 10
    • 11144337859 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 6553-6557.
    • (2004) Chem. Int. Ed , vol.43 , pp. 6553-6557
    • Angew1
  • 21
    • 0010667687 scopus 로고
    • Review
    • Review: Gutsche, C. D. Org. React. 1954, 8, 365-429.
    • (1954) Org. React , vol.8 , pp. 365-429
    • Gutsche, C.D.1
  • 32
    • 36649018642 scopus 로고    scopus 로고
    • 7,13 Exceptions exist for fluorinated derivatives.
    • 7,13 Exceptions exist for fluorinated derivatives.
  • 33
    • 85065231907 scopus 로고
    • For a compilation of methods, see: a
    • For a compilation of methods, see: (a) Krapcho, A. P. Synthesis 1974, 383-419.
    • (1974) Synthesis , pp. 383-419
    • Krapcho, A.P.1
  • 39
    • 13444299204 scopus 로고    scopus 로고
    • 2-triazolines, see: (a) Wohl, R. A. J. Org. Chem. 1973, 38, 3862-3864.
    • 2-triazolines, see: (a) Wohl, R. A. J. Org. Chem. 1973, 38, 3862-3864.
  • 41
    • 0001431840 scopus 로고
    • (c) Fitjer, L. Chem. Ber. 1982, 115, 1047-1060.
    • (1982) Chem. Ber , vol.115 , pp. 1047-1060
    • Fitjer, L.1
  • 44
    • 33947088106 scopus 로고    scopus 로고
    • An analogous rearrangement of 30 to 23 is known: Mundy, B. P, Otzenberger, R. D. J. Org. Chem. 1973, 38, 2109-2110
    • An analogous rearrangement of 30 to 23 is known: Mundy, B. P.; Otzenberger, R. D. J. Org. Chem. 1973, 38, 2109-2110.
  • 55
    • 0010633369 scopus 로고
    • For an alternative approach via addition of 1-ethoxycyclopropyl-lithium to carbonyl compounds, see: a
    • For an alternative approach via addition of 1-ethoxycyclopropyl-lithium to carbonyl compounds, see: (a) Gadwood, R. C.; Rubino, M. R.; Nagarajan, S. C.; Michel, S. T. J.Org. Chem. 1985, 50, 3255-3260.
    • (1985) J.Org. Chem , vol.50 , pp. 3255-3260
    • Gadwood, R.C.1    Rubino, M.R.2    Nagarajan, S.C.3    Michel, S.T.4
  • 60
    • 84912215075 scopus 로고    scopus 로고
    • 36b
    • 36b
  • 61
    • 33947477352 scopus 로고    scopus 로고
    • Synthesis of 1-bromo-cyclopentene: (a) Abell, P. I.; Chiao, C. J. Am. Chem. Soc. 1960, 82, 3610-3613.
    • Synthesis of 1-bromo-cyclopentene: (a) Abell, P. I.; Chiao, C. J. Am. Chem. Soc. 1960, 82, 3610-3613.
  • 62
    • 84942752381 scopus 로고    scopus 로고
    • Reductive lithiation: (b) Neumann, H.; Seebach, D. Chem. Ber. 1978, 111, 2785-2812.
    • Reductive lithiation: (b) Neumann, H.; Seebach, D. Chem. Ber. 1978, 111, 2785-2812.
  • 64
    • 0000337052 scopus 로고    scopus 로고
    • Synthesis of selenoketals: (a) Krief, A.; Clarembeau, M.; Cravador, A.; Dumont, W.; Hevesi, L.; Luchetti, J.; van Ende, D. Tetrahedron 1985, 41, 4793-4812.
    • Synthesis of selenoketals: (a) Krief, A.; Clarembeau, M.; Cravador, A.; Dumont, W.; Hevesi, L.; Luchetti, J.; van Ende, D. Tetrahedron 1985, 41, 4793-4812.
  • 65
    • 33745507572 scopus 로고
    • Reductive lithiations: (b) Krief, A
    • Reductive lithiations: (b) Krief, A. Tetrahedron 1980, 36, 2531-2540.
    • (1980) Tetrahedron , vol.36 , pp. 2531-2540
  • 69
    • 0000939113 scopus 로고
    • For a review on the chiroptical properties of carbonyl compounds, see
    • For a review on the chiroptical properties of carbonyl compounds, see: Kirk, D. N. Tetrahedron 1986, 42, 777-818.
    • (1986) Tetrahedron , vol.42 , pp. 777-818
    • Kirk, D.N.1
  • 73
    • 36649010111 scopus 로고    scopus 로고
    • TURBOMOLE 5.6; Ahlrichs, R. et al., Universität Karlsruhe, 2003. See also: http://www.turbomole.com.
    • TURBOMOLE 5.6; Ahlrichs, R. et al., Universität Karlsruhe, 2003. See also: http://www.turbomole.com.
  • 98
    • 36649036064 scopus 로고    scopus 로고
    • PC-Model 7.0, Serena Software, Bloomington, IN 47405.
    • PC-Model 7.0, Serena Software, Bloomington, IN 47405.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.