메뉴 건너뛰기




Volumn 2003, Issue 13, 2003, Pages 68-86

Microwave-assisted heterocyclic synthesis

Author keywords

Conventional heating; Heterocycles; Microwaves; Single mode technology

Indexed keywords

AMIDE; BENZENE DERIVATIVE; BENZIMIDAZOLE DERIVATIVE; BENZOTHIAZOLE DERIVATIVE; BENZOXAZOLE DERIVATIVE; C CARBAMOYL 1,2,3 TRIAZOLE DERIVATIVE; DIHYDROPYRIDINE DERIVATIVE; DIHYDROPYRIDOPYRIMIDINONE DERIVATIVE; DIHYDROPYRIMIDINE DERIVATIVE; GAMMA CARBOLINE DERIVATIVE; HETEROCYCLIC COMPOUND; IMIDAZOLE DERIVATIVE; INDOLE DERIVATIVE; ISOXAZOLINE DERIVATIVE; OXADIAZOLE DERIVATIVE; OXAZOLINE DERIVATIVE; PYRAZOLE DERIVATIVE; PYRAZOLINE DERIVATIVE; PYRIMIDO[1,2 A]PYRIMIDINE DERIVATIVE; PYRROLE DERIVATIVE; QUINOLINE DERIVATIVE; TETRAZINE DERIVATIVE; TETRAZOLE DERIVATIVE; TRANSITION ELEMENT; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 3242665367     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (75)

References (37)
  • 1
    • 0029078472 scopus 로고
    • Caddick, S. Tetrahedron 1995, 51, 10403. Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199. Lidström, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406. Fini, A.; Breccia, A. Pure Appl. Chem. 1999, 71, 573.
    • (1995) Tetrahedron , vol.51 , pp. 10403
    • Caddick, S.1
  • 2
    • 0035813242 scopus 로고    scopus 로고
    • Caddick, S. Tetrahedron 1995, 51, 10403. Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199. Lidström, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406. Fini, A.; Breccia, A. Pure Appl. Chem. 1999, 71, 573.
    • (2001) Tetrahedron , vol.57 , pp. 9199
    • Perreux, L.1    Loupy, A.2
  • 3
    • 0035813244 scopus 로고    scopus 로고
    • Caddick, S. Tetrahedron 1995, 51, 10403. Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199. Lidström, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406. Fini, A.; Breccia, A. Pure Appl. Chem. 1999, 71, 573.
    • (2001) Tetrahedron , vol.57 , pp. 9225
    • Lidström, P.1    Tierney, J.2    Wathey, B.3    Westman, J.4
  • 4
    • 0035341584 scopus 로고    scopus 로고
    • Caddick, S. Tetrahedron 1995, 51, 10403. Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199. Lidström, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406. Fini, A.; Breccia, A. Pure Appl. Chem. 1999, 71, 573.
    • (2001) Drug Discovery Today , vol.6 , pp. 406
    • Larhed, M.1    Hallberg, A.2
  • 5
    • 21044448696 scopus 로고    scopus 로고
    • Caddick, S. Tetrahedron 1995, 51, 10403. Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199. Lidström, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406. Fini, A.; Breccia, A. Pure Appl. Chem. 1999, 71, 573.
    • (1999) Pure Appl. Chem. , vol.71 , pp. 573
    • Fini, A.1    Breccia, A.2
  • 7
    • 0033444261 scopus 로고    scopus 로고
    • Loupy, A.; Petit, A.; Hamelin, J.; Texier-Boullet, F.; Jacquault, P.; Mathé, D. Synthesis 1998, 1213. Varma, R. S Green Chem. 1999, 1, 43. Kuhnert, N.; Danks, T. N. Green Chem. 2001, 3, 68. Tanaka, K.; Toda, F. Chem. Rev. 2000, 100, 1025.
    • (1999) Green Chem. , vol.1 , pp. 43
    • Varma, R.S.1
  • 8
    • 57249102965 scopus 로고    scopus 로고
    • Loupy, A.; Petit, A.; Hamelin, J.; Texier-Boullet, F.; Jacquault, P.; Mathé, D. Synthesis 1998, 1213. Varma, R. S Green Chem. 1999, 1, 43. Kuhnert, N.; Danks, T. N. Green Chem. 2001, 3, 68. Tanaka, K.; Toda, F. Chem. Rev. 2000, 100, 1025.
    • (2001) Green Chem. , vol.3 , pp. 68
    • Kuhnert, N.1    Danks, T.N.2
  • 9
    • 0000884192 scopus 로고    scopus 로고
    • Loupy, A.; Petit, A.; Hamelin, J.; Texier-Boullet, F.; Jacquault, P.; Mathé, D. Synthesis 1998, 1213. Varma, R. S Green Chem. 1999, 1, 43. Kuhnert, N.; Danks, T. N. Green Chem. 2001, 3, 68. Tanaka, K.; Toda, F. Chem. Rev. 2000, 100, 1025.
    • (2000) Chem. Rev. , vol.100 , pp. 1025
    • Tanaka, K.1    Toda, F.2
  • 10
    • 0012106816 scopus 로고    scopus 로고
    • CEM Publishing: Matthews, NC
    • Single-mode cavities offer more consistent and predictable energy distribution. Single-mode instruments produce one homogeneous, intense pocket of energy that is highly reproducible. Due to their uniform energy distribution and higher power density, these systems typically couple more efficiently with small samples. Hayes, B. L. Microwave Synthesis: Chemistry at the Speed of Light; CEM Publishing: Matthews, NC, 2002.
    • (2002) Microwave Synthesis: Chemistry at the Speed of Light
    • Hayes, B.L.1
  • 33
    • 0001142573 scopus 로고
    • Häbich, D.; Barth, W.; Rösner, M. Heterocycles 1989, 29, 2083. Mearman, R. C.; Newall, C. E.; Tonge, A. P. J. Antibiot. 1984, 37, 885. Olesen, P. H.; Nielsen, F. E.; Pedersen, E. B.; Becher, J. J. Heterocycl. Chem. 1984, 21, 1603.
    • (1989) Heterocycles , vol.29 , pp. 2083
    • Häbich, D.1    Barth, W.2    Rösner, M.3
  • 34
    • 0021182726 scopus 로고
    • Häbich, D.; Barth, W.; Rösner, M. Heterocycles 1989, 29, 2083. Mearman, R. C.; Newall, C. E.; Tonge, A. P. J. Antibiot. 1984, 37, 885. Olesen, P. H.; Nielsen, F. E.; Pedersen, E. B.; Becher, J. J. Heterocycl. Chem. 1984, 21, 1603.
    • (1984) J. Antibiot. , vol.37 , pp. 885
    • Mearman, R.C.1    Newall, C.E.2    Tonge, A.P.3
  • 36
    • 3242701116 scopus 로고    scopus 로고
    • note
    • Unpublished results from authors' laboratory.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.