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Volumn 13, Issue 16, 2011, Pages 4324-4327

Iodonium salts are key intermediates in Pd-catalyzed acetoxylation of pyrroles

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EID: 80051705553     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol201665c     Document Type: Article
Times cited : (44)

References (53)
  • 26
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    • It has been shown that cyclopalladation is the rate-limiting step of the acetoxylation reaction
    • It has been shown that cyclopalladation is the rate-limiting step of the acetoxylation reaction: Stowers, K. J.; Sanford, M. S. Org. Lett. 2009, 11, 4584
    • (2009) Org. Lett. , vol.11 , pp. 4584
    • Stowers, K.J.1    Sanford, M.S.2
  • 29
    • 34250315396 scopus 로고    scopus 로고
    • The 3-hydroxypyrrole subunit is incorporated into Obatoclax, an experimental drug candidate for the treatment of various types of cancer: Substituted 3-hydroxypyrroles have also been employed
    • The 3-hydroxypyrrole subunit is incorporated into Obatoclax, an experimental drug candidate for the treatment of various types of cancer: Drugs Future, 2007, 32, 228. Substituted 3-hydroxypyrroles have also been employed
    • (2007) Drugs Future , vol.32 , pp. 228
  • 31
    • 80051698392 scopus 로고    scopus 로고
    • Chem. Abstr. 2005, 142, 197868.
    • (2005) Chem. Abstr. , vol.142 , pp. 197868
  • 39
    • 0033525502 scopus 로고    scopus 로고
    • Single report on preparation of pyrrolyl-3-iodonium triflates from 3-trimethylsilylpyrrole
    • Single report on preparation of pyrrolyl-3-iodonium triflates from 3-trimethylsilylpyrrole: Liu, J.-H.; Chan, H.-W.; Xue, F.; Wang, Q.-G.; Mak, T. C. W.; Wong, H. N. C. J. Org. Chem. 1999, 64, 1630
    • (1999) J. Org. Chem. , vol.64 , pp. 1630
    • Liu, J.-H.1    Chan, H.-W.2    Xue, F.3    Wang, Q.-G.4    Mak, T.C.W.5    Wong, H.N.C.6
  • 40
    • 77955471751 scopus 로고    scopus 로고
    • Correlation between yields of phenyliodonium salts and Hammett σ constants of substituents has been reported: See also the Supporting Information, p S26
    • Correlation between yields of phenyliodonium salts and Hammett σ constants of substituents has been reported: Dohi, T.; Yamaoka, N.; Kita, Y. Tetrahedron 2010, 66, 5775. See also the Supporting Information, p S26
    • (2010) Tetrahedron , vol.66 , pp. 5775
    • Dohi, T.1    Yamaoka, N.2    Kita, Y.3
  • 41
    • 0004061172 scopus 로고    scopus 로고
    • EAr reactions of pyrroles, see: 5 th ed. John Wiley & Sons: Chichester
    • EAr reactions of pyrroles, see: Joule, J. A.; Mills, K. Heterocyclic Chemistry, 5 th ed.; John Wiley & Sons: Chichester, 2010; pp 289-323.
    • (2010) Heterocyclic Chemistry , pp. 289-323
    • Joule, J.A.1    Mills, K.2
  • 48
    • 34047101384 scopus 로고    scopus 로고
    • references cited therein
    • Deprez, N. R.; Sanford, M. S. Inorg. Chem. 2007, 46, 1924 and references cited therein
    • (2007) Inorg. Chem. , vol.46 , pp. 1924
    • Deprez, N.R.1    Sanford, M.S.2
  • 49
    • 0032576186 scopus 로고    scopus 로고
    • 2-coordination of 2-tributylstannylfurane to Pd(II) followed by tin-to-palladium transmetallation of the furyl group has been observed
    • 2-coordination of 2-tributylstannylfurane to Pd(II) followed by tin-to-palladium transmetallation of the furyl group has been observed: Cotter, W. D.; Barbour, L.; McNamara, K. L.; Hechter, R.; Lachicotte, R. J. J. Am. Chem. Soc. 1998, 120, 11016
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11016
    • Cotter, W.D.1    Barbour, L.2    McNamara, K.L.3    Hechter, R.4    Lachicotte, R.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.