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Volumn 5, Issue 1, 2003, Pages 55-57

Synthesis of homoallyl ethers via allylation of acetals in ionic liquids catalyzed by trimethylsilyl trifluoromethanesulfonate

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; DICHLOROMETHANE; ETHER DERIVATIVE; SOLVENT; SULFONIC ACID DERIVATIVE; TRIMETHYLSILYLTRIFLUOROMETHANESULFONATE; UNCLASSIFIED DRUG;

EID: 0141744973     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0271739     Document Type: Article
Times cited : (133)

References (30)
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    • Garrett R. L.; DeVito, S. C. In Designing Safer Chemicals; American Chemical Society Symposium Series 640; American Chemical Society: Washington, DC, 1996; Chapter 1.
    • (1996) Designing Safer Chemicals
    • Garrett, R.L.1    DeVito, S.C.2
  • 19
    • 0000034575 scopus 로고    scopus 로고
    • For reviews on ionic liquids, see: (a) Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. (b) Welton, T. Chem. Rev. 1999, 99, 2071-2083. (c) Gordon, C. M. Appl. Catal. A: General 2001, 222, 101-117. (d) Butler, R. Chem. Ind. (London) 2001, 17, 532. (e) Wasserscheid, P. Nachr. Chem. 2001, 49, 12-16.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3772
    • Wasserscheid, P.1    Keim, W.2
  • 20
    • 0347417134 scopus 로고    scopus 로고
    • For reviews on ionic liquids, see: (a) Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. (b) Welton, T. Chem. Rev. 1999, 99, 2071-2083. (c) Gordon, C. M. Appl. Catal. A: General 2001, 222, 101-117. (d) Butler, R. Chem. Ind. (London) 2001, 17, 532. (e) Wasserscheid, P. Nachr. Chem. 2001, 49, 12-16.
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2083
    • Welton, T.1
  • 21
    • 0035923960 scopus 로고    scopus 로고
    • For reviews on ionic liquids, see: (a) Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. (b) Welton, T. Chem. Rev. 1999, 99, 2071-2083. (c) Gordon, C. M. Appl. Catal. A: General 2001, 222, 101-117. (d) Butler, R. Chem. Ind. (London) 2001, 17, 532. (e) Wasserscheid, P. Nachr. Chem. 2001, 49, 12-16.
    • (2001) Appl. Catal. A: General , vol.222 , pp. 101-117
    • Gordon, C.M.1
  • 22
    • 0000034575 scopus 로고    scopus 로고
    • For reviews on ionic liquids, see: (a) Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. (b) Welton, T. Chem. Rev. 1999, 99, 2071-2083. (c) Gordon, C. M. Appl. Catal. A: General 2001, 222, 101-117. (d) Butler, R. Chem. Ind. (London) 2001, 17, 532. (e) Wasserscheid, P. Nachr. Chem. 2001, 49, 12-16.
    • (2001) Chem. Ind. (London) , vol.17 , pp. 532
    • Butler, R.1
  • 23
    • 19244381151 scopus 로고    scopus 로고
    • For reviews on ionic liquids, see: (a) Wasserscheid, P.; Keim, W. Angew. Chem., Int. Ed. 2000, 39, 3772. (b) Welton, T. Chem. Rev. 1999, 99, 2071-2083. (c) Gordon, C. M. Appl. Catal. A: General 2001, 222, 101-117. (d) Butler, R. Chem. Ind. (London) 2001, 17, 532. (e) Wasserscheid, P. Nachr. Chem. 2001, 49, 12-16.
    • (2001) Nachr. Chem. , vol.49 , pp. 12-16
    • Wasserscheid, P.1
  • 26
    • 0141471379 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis, there was no evidence of either ionic liquid in the ether layer or any organic product in the ionic liquid.
  • 27
    • 0141583020 scopus 로고    scopus 로고
    • note
    • 6], such as etching of the glassware.
  • 28
    • 0141583018 scopus 로고    scopus 로고
    • note
    • The ionic liquids were dried as follows after each run: The recovered ionic liquid was stirred over powdered activated 4 Å sieves for 12 h, dissolved in ethyl acetate, and filtered, and the solvent was removed on a rotary evaporator. The ionic liquid was further dried by heating at 70°C (0.1 mmHg) for 4 h.
  • 29
    • 0141583019 scopus 로고    scopus 로고
    • note
    • 2 requires 205.12296 (M + 1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.