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Volumn 50, Issue 51, 2011, Pages 12236-12239

Synergistic palladium-catalyzed C(sp 3)-H Activation/C(sp 3)-O bond formation: A direct, step-economical route to benzolactones

Author keywords

amino acids; benzolactones; C H activation; homogeneous catalysis; palladium

Indexed keywords

BENZOLACTONES; BOND FORMATION; C-H ACTIVATION; HOMOGENEOUS CATALYSIS; ONE STEP; PROTECTING GROUP; SUBSTITUTION PATTERNS;

EID: 83755173391     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201105894     Document Type: Article
Times cited : (176)

References (66)
  • 6
    • 72449170089 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9792-9826011
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9792-9826011
  • 8
    • 67649488045 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5094-5115.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5094-5115
  • 22
    • 69549090264 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6892-6895
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6892-6895
  • 29
    • 84855488446 scopus 로고    scopus 로고
    • Platinum is more expensive than palladium (10.000$/mol versus 1500$/mol, respectively)
    • Platinum is more expensive than palladium (10.000$/mol versus 1500$/mol, respectively).
  • 31
    • 84855482730 scopus 로고    scopus 로고
    • 3)-O bonds was reported
    • 3)-O bonds was reported:, S. L. Marquard, J. F. Hartwig, Angew. Chem. 2011, 123, 7257-7261
    • (2011) Angew. Chem. , vol.123 , pp. 7257-7261
    • Marquard, S.L.1    Hartwig, J.F.2
  • 32
    • 79960634633 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 7119-7123.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7119-7123
  • 33
    • 77954612360 scopus 로고    scopus 로고
    • For a review on reductive elmininations of high-valent species to C-O bonds, see
    • For a review on reductive elmininations of high-valent species to C-O bonds, see:, A. N. Vedernikov, Top. Organomet. Chem. 2010, 31, 101.
    • (2010) Top. Organomet. Chem. , vol.31 , pp. 101
    • Vedernikov, A.N.1
  • 36
    • 84855503276 scopus 로고    scopus 로고
    • 3)-H bonds, see
    • 3)-H bonds, see
  • 40
    • 70349777759 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6097-6100
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6097-6100
  • 51
    • 48849108176 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4882-4886.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4882-4886
  • 54
    • 83755168216 scopus 로고    scopus 로고
    • Future investigations are aimed at improving catalyst performance as unreacted starting material was recovered from reactions with 50-70-% yield
    • Future investigations are aimed at improving catalyst performance as unreacted starting material was recovered from reactions with 50-70-% yield.
  • 55
    • 84855516407 scopus 로고    scopus 로고
    • For an elegant macrolactonization method initiated by C-H oxidation by π-allyl intermediates, see Ref. [4d]
    • For an elegant macrolactonization method initiated by C-H oxidation by π-allyl intermediates, see Ref. [4d].
  • 56
    • 83755170751 scopus 로고    scopus 로고
    • A substituent at the 5-position was required for selectively activating the benzylic C-H bond. Indeed, the reaction of the corresponding ortho-methylbenzoic acid did not afford any benzolactone at all
    • A substituent at the 5-position was required for selectively activating the benzylic C-H bond. Indeed, the reaction of the corresponding ortho-methylbenzoic acid did not afford any benzolactone at all.
  • 57
    • 83755180737 scopus 로고    scopus 로고
    • No conversion to products was observed
    • No conversion to products was observed.
  • 63
  • 64
    • 73249135129 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9412-9423.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9412-9423
  • 66
    • 84855487948 scopus 로고    scopus 로고
    • 3)-H activation via benzylic radicals
    • 3)-H activation via benzylic radicals.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.