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Volumn 350, Issue 4, 2008, Pages 565-569

Catalytic dehydrogenation of o-alkylated or o-alkoxylated iodoarenes with concomitant hydrogenolysis

Author keywords

C H activation; Catalysis; Dehydrogenation; Palladium

Indexed keywords


EID: 53849109561     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700562     Document Type: Article
Times cited : (30)

References (34)
  • 12
    • 0042728760 scopus 로고
    • For the preferential transformation of an aromatic over an aliphatic C-H bond, see, for example
    • For the preferential transformation of an aromatic over an aliphatic C-H bond, see, for example: A. D. Ryabov, Chem. Rev. 1990, 90, 403.
    • (1990) Chem. Rev , vol.90 , pp. 403
    • Ryabov, A.D.1
  • 16
    • 0007689590 scopus 로고
    • The acetate anion was reported to favor norbornene insertion. See, for example
    • The acetate anion was reported to favor norbornene insertion. See, for example: M. C. Gallazzi, L. Porri, G. Vitulli, J. Organomet. Chem. 1975, 97, 131.
    • (1975) J. Organomet. Chem , vol.97 , pp. 131
    • Gallazzi, M.C.1    Porri, L.2    Vitulli, G.3
  • 18
    • 33845938814 scopus 로고    scopus 로고
    • and references cited therein. For a rational interpretation of the use of bases see
    • For a rational interpretation of the use of bases see: M. Lafrance, A. K. Fagnou, J. Am. Chem. Soc. 2006, 128, 16496, and references cited therein.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 16496
    • Lafrance, M.1    Fagnou, A.K.2
  • 19
    • 53849130481 scopus 로고    scopus 로고
    • To our knowledge compounds of type 10 and 11 have not been prepared so far under the conditions of a conventional Heck reaction from aryl vinyl ethers, probably owing to the instability of the latter.
    • To our knowledge compounds of type 10 and 11 have not been prepared so far under the conditions of a conventional Heck reaction from aryl vinyl ethers, probably owing to the instability of the latter.
  • 20
    • 53849122150 scopus 로고    scopus 로고
    • Analogously, no double bond formation was obtained under our conditions with substituents offering steric hindrance or unsuitable conformation such as for example o,o-diethyl and o,o-diisopropyl.
    • Analogously, no double bond formation was obtained under our conditions with substituents offering steric hindrance or unsuitable conformation such as for example o,o-diethyl and o,o-diisopropyl.
  • 21
    • 33644905281 scopus 로고    scopus 로고
    • For a review on intramolecular arylation of arenes, see
    • For a review on intramolecular arylation of arenes, see: L.-C. Campeau, K. Fagnou, Chem. Commun. 2006, 1253.
    • (2006) Chem. Commun , pp. 1253
    • Campeau, L.-C.1    Fagnou, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.