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Volumn 4, Issue , 2008, Pages

Convenient method for preparing benzyl ethers and esters using 2-benzyloxypyridine

Author keywords

Alcohols; Alkylation; Benzyl; Electrophilic substitution; Esters; Ethers; Protecting groups; Reagent

Indexed keywords


EID: 78650409021     PISSN: None     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.4.44     Document Type: Article
Times cited : (19)

References (35)
  • 6
    • 33646520636 scopus 로고    scopus 로고
    • doi:10.1021/jo0602773
    • Poon, K. W. C.; Dudley, G. B. J. Org. Chem. 2006, 71, 3923-3927. doi:10.1021/jo0602773
    • (2006) J. Org. Chem. , vol.71 , pp. 3923-3927
    • Poon, K.W.C.1    Dudley, G.B.2
  • 7
    • 29744438054 scopus 로고    scopus 로고
    • A bench-stable organic salt for the benzylation of alcohols
    • DOI 10.1055/s-2005-921898, S08705ST
    • Poon, K. W. C.; House, S. E.; Dudley, G. B. Synlett 2005, 3142-3144. doi:10.1055/s-2005-921898 (Pubitemid 43029953)
    • (2005) Synlett , Issue.20 , pp. 3142-3144
    • Poon, K.W.C.1    House, S.E.2    Dudley, G.B.3
  • 11
    • 33646535889 scopus 로고
    • Benzyl 2,2,2-trichloroacetimidate
    • Paquette, L. A., Ed.; John Wiley & Sons: New York, N.Y.
    • Boa, A. N.; Jenkins, P. R. Benzyl 2,2,2-Trichloroacetimidate. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley & Sons: New York, N.Y., 1995; Vol. 1, pp 374-375.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , vol.1 , pp. 374-375
    • Boa, A.N.1    Jenkins, P.R.2
  • 12
    • 83455255052 scopus 로고    scopus 로고
    • 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate
    • Paquette, L. A.; Crich, D.; Fuchs, P.; Molander, G., Eds.; John Wiley & Sons, Posted September 15, (accessed November 24, 2008). doi:10.1002/047084289X.rn00906
    • Dudley, G. B. 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate. In e-EROS Encylopedia of Reagents for Organic Synthesis [Online]; Paquette, L. A.; Crich, D.; Fuchs, P.; Molander, G., Eds.; John Wiley & Sons, Posted September 15, 2008. http://mrw.interscience.wiley.com/eros/articles/rn00906/ frame.html (accessed November 24, 2008). doi:10.1002/047084289X.rn00906.
    • (2008) E-EROS Encylopedia of Reagents for Organic Synthesis
    • Dudley, G.B.1
  • 14
    • 37549039126 scopus 로고    scopus 로고
    • doi:10.1021/jo701968d
    • Legeay, J.-C.; Langlois, N. J. Org. Chem. 2007, 72, 10108-10113. doi:10.1021/jo701968d
    • (2007) J. Org. Chem. , vol.72 , pp. 10108-10113
    • Legeay, J.-C.1    Langlois, N.2
  • 15
    • 33845465260 scopus 로고    scopus 로고
    • Stereoselective formal synthesis of the potent proteasome inhibitor: salinosporamide A
    • DOI 10.1016/j.tetlet.2006.11.087, PII S0040403906022970
    • Caubert, V.; Massé, J.; Retailleau, P.; Langlois, N. Tetrahedron Lett. 2007, 48, 381-384. doi:10.1016/j.tetlet.2006.11.087 (Pubitemid 44894512)
    • (2007) Tetrahedron Letters , vol.48 , Issue.3 , pp. 381-384
    • Caubert, V.1    Masse, J.2    Retailleau, P.3    Langlois, N.4
  • 17
    • 84876258974 scopus 로고    scopus 로고
    • Sigma-Aldrich catalog number 679674
    • Sigma-Aldrich catalog number 679674.
  • 19
    • 33947634131 scopus 로고    scopus 로고
    • Synthesis of para-methoxybenzyl (PMB) ethers under neutral conditions
    • DOI 10.1039/b617926f
    • Nwoye, E. O.; Dudley, G. B. Chem. Commun. 2007, 1436-1437. doi:10.1039/b617926f (Pubitemid 46496526)
    • (2007) Chemical Communications , Issue.14 , pp. 1436-1437
    • Nwoye, E.O.1    Dudley, G.B.2
  • 20
    • 35948952320 scopus 로고    scopus 로고
    • Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate
    • DOI 10.1021/jo7018625
    • Tummatorn, J.; Albiniak, P. A.; Dudley, G. B. J. Org. Chem. 2007, 72, 8962-8964. doi:10.1021/jo7018625 (Pubitemid 350071733)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.23 , pp. 8962-8964
    • Tummatorn, J.1    Albiniak, P.A.2    Dudley, G.B.3
  • 22
    • 35348912446 scopus 로고    scopus 로고
    • Thermally generated phenylcarbenium ions: acid-free and self-quenching Friedel-Crafts reactions
    • DOI 10.1016/j.tetlet.2007.09.116, PII S0040403907019028
    • Albiniak, P. A.; Dudley, G. B. Tetrahedron Lett. 2007, 48, 8097-8100. doi:10.1016/j.tetlet.2007.09.116 (Pubitemid 47575664)
    • (2007) Tetrahedron Letters , vol.48 , Issue.46 , pp. 8097-8100
    • Albiniak, P.A.1    Dudley, G.B.2
  • 23
    • 0000974143 scopus 로고    scopus 로고
    • doi:10.1021/jo9620324
    • Ogawa, A.; Curran, D. P. J. Org. Chem. 1997, 62, 450-451. doi:10.1021/jo9620324
    • (1997) J. Org. Chem. , vol.62 , pp. 450-451
    • Ogawa, A.1    Curran, D.P.2
  • 24
    • 0037415466 scopus 로고    scopus 로고
    • Efficient synthesis of optically active α-substituted glutamate analogs possessing α-hydroxymethyl and α-alkoxymethyl groups
    • DOI 10.1016/S0040-4039(02)02810-1, PII S0040403902028101
    • Kawasaki, M.; Namba, K.; Tsujishima, H.; Shinada, T.; Ohfune, Y. Tetrahedron Lett. 2003, 44, 1235-1238. doi:10.1016/S0040-4039(02)02810-1 (Pubitemid 36144143)
    • (2003) Tetrahedron Letters , vol.44 , Issue.6 , pp. 1235-1238
    • Kawasaki, M.1    Namba, K.2    Tsujishima, H.3    Shinada, T.4    Ohfune, Y.5
  • 27
    • 0017766655 scopus 로고
    • doi:10.1021/jo00423a027
    • Yamashiro, D. J. Org. Chem. 1977, 42, 523-525. doi:10.1021/jo00423a027
    • (1977) J. Org. Chem. , vol.42 , pp. 523-525
    • Yamashiro, D.1
  • 28
    • 0030867017 scopus 로고    scopus 로고
    • Para-Chlorobenzyl protecting groups as stabilizers of the glycosidic linkage: Synthesis of the 3-O-Sulfated lewis X trisaccharide
    • DOI 10.1016/S0040-4039(97)01670-5, PII S0040403997016705
    • Pohl, N. L.; Kiessling, L. L. Tetrahedron Lett. 1997, 38, 6985-6988. doi:10.1016/S0040-4039(97)01670-5 (Pubitemid 27402171)
    • (1997) Tetrahedron Letters , vol.38 , Issue.40 , pp. 6985-6988
    • Pohl, N.L.1    Kiessling, L.L.2
  • 33
    • 0343643766 scopus 로고
    • 2-Chloro-1-methylpyridinium Iodide
    • Paquette, L. A., Ed.; John Wiley & Sons: New York, N.Y.
    • Armstrong, A. 2-Chloro-1-methylpyridinium Iodide. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley & Sons: New York, N.Y., 1995; Vol. 2, pp 1174-1175.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , vol.2 , pp. 1174-1175
    • Armstrong, A.1
  • 35
    • 39349091263 scopus 로고    scopus 로고
    • An efficient means for generating p-methoxybenzyl (PMB) ethers under mildly acidic conditions
    • DOI 10.1055/s-2008-1032132
    • Stewart, C. A.; Peng, X.; Paquette, L. A. Synthesis 2008, 433-437. doi:10.1055/s-2008-1032132 (Pubitemid 351262990)
    • (2008) Synthesis , Issue.3 , pp. 0433-0437
    • Stewart, C.A.1    Peng, X.2    Paquette, L.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.