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Volumn 63, Issue 2, 2007, Pages 469-473

Solvent-free direct regioselective ring opening of epoxides with imidazoles

Author keywords

Benzimidazole; Epoxides; Imidazole; Nucleophilic attack; Ring opening

Indexed keywords

1 (1H BENZIMIDAZOL 1 YL) 2 METHYL 2 PROPANOL; 1 (1H BENZIMIDAZOL 1 YL) 2 OCTANOL; 1 (1H BENZIMIDAZOL 1 YL) 3 PHENOXY 2 PROPANOL; 1 (1H BENZIMIDAZOL 1 YL) 3 PHENYL 2 PROPANOL; 2 (1H BENZIMIDAZOL 1 YL) 1 PHENYLETHANOL; 2 (1H BENZIMIDAZOL 1 YL)CYCLOHEXANOL; BENZIMIDAZOLE DERIVATIVE; EPOXIDE; IMIDAZOLE DERIVATIVE; SOLVENT;

EID: 33751528525     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.10.055     Document Type: Article
Times cited : (58)

References (26)
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  • 11
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    • In the framework of asymmetric synthesis, the use of chiral catalysts becomes an interesting method of performing asymmetric ring opening (ARO) of epoxides, see review:
    • In the framework of asymmetric synthesis, the use of chiral catalysts becomes an interesting method of performing asymmetric ring opening (ARO) of epoxides, see review:. Pastor I.M., and Yus M. Curr. Org. Chem. 9 (2005) 1-29
    • (2005) Curr. Org. Chem. , vol.9 , pp. 1-29
    • Pastor, I.M.1    Yus, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.