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Volumn 75, Issue 24, 2010, Pages 8666-8669

Practical synthesis of functionalized 1,5-disubstituted 1,2,4-triazole derivatives

Author keywords

[No Author keywords available]

Indexed keywords

DIRECT REACTIONS; FUNCTIONALIZED; GENERAL APPROACH; GOOD YIELD; HYDROCHLORIDE SALTS; MILD REACTION CONDITIONS; NMR SPECTROSCOPY; OPTIMIZED CONDITIONS; STABLE CRYSTALLINE SOLIDS; TRIAZOLE DERIVATIVES;

EID: 78650343266     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1017603     Document Type: Article
Times cited : (38)

References (61)
  • 12
    • 33745611785 scopus 로고    scopus 로고
    • Selected examples of the synthesis of 1,2,4-triazole rings
    • Selected examples of the synthesis of 1,2,4-triazole rings: Bekircan, O.; Bektas, H. Molecules 2006, 11, 469-477
    • (2006) Molecules , vol.11 , pp. 469-477
    • Bekircan, O.1    Bektas, H.2
  • 33
    • 77951210911 scopus 로고    scopus 로고
    • For review for the synthesis of 3,4,5-trisubstituted-1,2,4-triazol, see:;, For review of 1,2,4-triazole chemistry, see: Chem. Rev. 1961, 61, 87-127
    • For review for the synthesis of 3,4,5-trisubstituted-1,2,4-triazol, see: Moulin, A.; Bibian, M.; Blayo, A.-L.; Habnouni, S. E.; Martinez, J.; Fehrentz, J.-A. Chem. Rev. 2010, 110, 1809-1827 For review of 1,2,4-triazole chemistry, see: Potts, K. T. Chem. Rev. 1961, 61, 87-127
    • (2010) Chem. Rev. , vol.110 , pp. 1809-1827
    • Moulin, A.1    Bibian, M.2    Blayo, A.-L.3    Habnouni, S.E.4    Martinez, J.5    Fehrentz, J.-A.6    Potts, K.T.7
  • 35
    • 0002995611 scopus 로고
    • For synthesis of 1,2,4-triazole ring through amidines, please see
    • For synthesis of 1,2,4-triazole ring through amidines, please see: Pérez, M. A.; Dorado, C. A.; Soto, J. L. Synthesis 1983, 6, 483-486
    • (1983) Synthesis , vol.6 , pp. 483-486
    • Pérez, M.A.1    Dorado, C.A.2    Soto, J.L.3
  • 38
    • 0019792144 scopus 로고
    • For synthesis of 1,2,4-triazole ring through isothiocyanates, please see
    • For synthesis of 1,2,4-triazole ring through isothiocyanates, please see: Ogura, H.; Takahashi, H.; Sato, O. Chem. Pharm. Bull. 1981, 29, 2188-2192
    • (1981) Chem. Pharm. Bull. , vol.29 , pp. 2188-2192
    • Ogura, H.1    Takahashi, H.2    Sato, O.3
  • 58
    • 78650333973 scopus 로고    scopus 로고
    • the case of amine substrates, 2.1 equiv of 6 can be used to avoid the use of any additional base
    • In the case of amine substrates, 2.1 equiv of 6 can be used to avoid the use of any additional base.
  • 59
    • 78650330658 scopus 로고
    • Patent DE 3125438 A1
    • Klug, H. Ger. Offen. 1983, Patent DE 3125438 A1.
    • (1983) Ger. Offen.
    • Klug, H.1
  • 61
    • 78650364596 scopus 로고    scopus 로고
    • Reactions in solvents like DMF, DMSO, or NMP gave full conversions within similar reaction time. However, minor loss of desired product in aqueous workup was observed. In addition, a slighly lower assay yield (HPLC) was sometimes obtained in these solvents than in the reaction conducted in IPA
    • Reactions in solvents like DMF, DMSO, or NMP gave full conversions within similar reaction time. However, minor loss of desired product in aqueous workup was observed. In addition, a slighly lower assay yield (HPLC) was sometimes obtained in these solvents than in the reaction conducted in IPA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.