메뉴 건너뛰기




Volumn 37, Issue 6, 2004, Pages 553-564

Conformational and structural analysis of 6-(4-methoxy-phenyl)-1,5,7a- triphenyl-tetrahydro-imidazo[1,5-b][1,2,4]oxadiazol-2-one

Author keywords

1,3 dipolar cycloaddition; cis imidazo 1,5 b 1,2,4 oxadiazol 2 one; Crystal structure; PM3

Indexed keywords

6 (4 METHOXYPHENYL)1,5,7A TRIPHENYL TETRAHYDROIMIDAZO[1,5 B][1,2,4]OXADIAZOL 2 ONE; OXADIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 8744221603     PISSN: 00387010     EISSN: None     Source Type: Journal    
DOI: 10.1081/SL-200036390     Document Type: Article
Times cited : (1)

References (19)
  • 2
    • 84982443772 scopus 로고
    • Intramolecular 1,3-dipolar cycloaddition reactions
    • Padwa, A. Intramolecular 1,3-dipolar cycloaddition reactions. Angew. Chem. Int. Ed. Eng. 1976, 15, 123-180.
    • (1976) Angew. Chem. Int. Ed. Eng. , vol.15 , pp. 123-180
    • Padwa, A.1
  • 3
    • 84980167410 scopus 로고
    • Intramolecular [4 + 2] and [3 + 2] cycloaddition in organic synthesis
    • Oppolzer, W. Intramolecular [4 + 2] and [3 + 2] cycloaddition in organic synthesis. Angew. Chem. Int. Ed. Eng. 1977, 16, 10-23.
    • (1977) Angew. Chem. Int. Ed. Eng. , vol.16 , pp. 10-23
    • Oppolzer, W.1
  • 4
    • 84989463058 scopus 로고
    • 1,3-Dipolar cycloaddition reactions of nitrones
    • Black, D.St.C.; Crozier, R.F.; Davis, V.C. 1,3-Dipolar cycloaddition reactions of nitrones. Synthesis 1975, 205-221.
    • (1975) Synthesis , pp. 205-221
    • Black, D.St.C.1    Crozier, R.F.2    Davis, V.C.3
  • 5
    • 0037988226 scopus 로고    scopus 로고
    • Regio and diastereoselective addition of imidazole 3-oxides aryl isocyanates
    • Coşkun, N. Regio and diastereoselective addition of imidazole 3-oxides aryl isocyanates. Tetrahedron 1997, 53, 13873-13882.
    • (1997) Tetrahedron , vol.53 , pp. 13873-13882
    • Coşkun, N.1
  • 6
    • 0031592590 scopus 로고    scopus 로고
    • Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates
    • Coşkun, N. Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates. Tetrahedron Lett. 1997, 38, 2299-2302.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 2299-2302
    • Coşkun, N.1
  • 8
    • 0038664703 scopus 로고    scopus 로고
    • The first examples of di- and cis triaryl-3a,4,5,6-tetrahydroimidazo[1,5- b] isoxazoles and their ring-opening reactions
    • Coşkun, N.; Tat, F.T.; Güven, Ö.Ö.; Ülkü, D.; Arici, C. The first examples of di- and cis triaryl-3a,4,5,6- tetrahydroimidazo[1,5-b] isoxazoles and their ring-opening reactions. Tetrahedron Lett. 2000, 41, 5407-5409.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5407-5409
    • Coşkun, N.1    Tat, F.T.2    Güven, Ö.Ö.3    Ülkü, D.4    Arici, C.5
  • 9
    • 0043157645 scopus 로고    scopus 로고
    • Organocatalysts promote enantioselective 1,3-dipolar cycloadditions of nitrones with 1-cycloalkene-1-carboxaldehydes
    • Karlsson, S.; Hoegberg, Hans-Erik. Organocatalysts promote enantioselective 1,3-dipolar cycloadditions of nitrones with 1-cycloalkene-1-carboxaldehydes. Eur. J. Org. Chem. 2003, 34, 2782-2791.
    • (2003) Eur. J. Org. Chem. , vol.34 , pp. 2782-2791
    • Karlsson, S.1    Hoegberg, H.-E.2
  • 10
    • 0007305682 scopus 로고    scopus 로고
    • Regioselectivity and diastereoselectivity in the 1,3-dipolar cycloadditions of nitrones with acrylnitrile and maleonitrile. The origin of ENDO/EXO selectivity
    • Rastelli, A.; Gandolfi, R.; Amade, M.S. Regioselectivity and diastereoselectivity in the 1,3-dipolar cycloadditions of nitrones with acrylnitrile and maleonitrile. The origin of ENDO/EXO selectivity. Adv. Quant. Chem. 1999, 36, 151-167.
    • (1999) Adv. Quant. Chem. , vol.36 , pp. 151-167
    • Rastelli, A.1    Gandolfi, R.2    Amade, M.S.3
  • 11
    • 0032540703 scopus 로고    scopus 로고
    • Catalytic enantioselective 1,3-dipolar cycloadditons between nitrones and alkenes using a novel heterochiral ytterbium(III) catalyst
    • Obayashi, S.; Kawamura, M. Catalytic enantioselective 1,3-dipolar cycloadditons between nitrones and alkenes using a novel heterochiral ytterbium(III) catalyst. J. Am. Chem. Soc. 1998, 120, 5840-5841.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5840-5841
    • Obayashi, S.1    Kawamura, M.2
  • 12
    • 0036027099 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloaddition reactions of carbohydrates derived nitrones and oximes
    • Osborn, H.M.L.; Gemmell, N.; Harwood, L.M.J. 1,3-Dipolar cycloaddition reactions of carbohydrates derived nitrones and oximes. Chem. Soc., Perkin Trans. 2002, 1, 2419.
    • (2002) Chem. Soc., Perkin Trans. , vol.1 , pp. 2419
    • Osborn, H.M.L.1    Gemmell, N.2    Harwood, L.M.J.3
  • 14
    • 84988073214 scopus 로고
    • Optimization of parameters for semiempirical methods II applications
    • Stewart, J.J.P. Optimization of parameters for semiempirical methods II applications. J. Comput. Chem. 1989, 10, 221-264.
    • (1989) J. Comput. Chem. , vol.10 , pp. 221-264
    • Stewart, J.J.P.1
  • 15
    • 84988129057 scopus 로고
    • Optimization of parameters for semiempirical methods I. Method
    • Stewart, J.J.P. Optimization of parameters for semiempirical methods I. method. J. Comput. Chem. 1989, 10, 209-220.
    • (1989) J. Comput. Chem. , vol.10 , pp. 209-220
    • Stewart, J.J.P.1
  • 16
    • 2342430094 scopus 로고
    • New developments in molecular orbital theory
    • Roothaan, C.C.J. New developments in molecular orbital theory. Rev. Mod. Phys. 1951, 23, 69-89.
    • (1951) Rev. Mod. Phys. , vol.23 , pp. 69-89
    • Roothaan, C.C.J.1
  • 19
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for Windows - A version of ORTEP-III with a graphical user interface (GUI)
    • Farrugia, L.J. ORTEP-3 for Windows - a version of ORTEP-III with a graphical user interface (GUI). J. Appl. Cryst. 1997, 30, 565.
    • (1997) J. Appl. Cryst. , vol.30 , pp. 565
    • Farrugia, L.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.