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Volumn 73, Issue 19, 2008, Pages 7800-7802

Sterically hindered benzophenones via rhodium-catalyzed oxidative arylation of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ALDEHYDES; AROMATIC COMPOUNDS; CHEMICAL REACTIONS; ORGANIC COMPOUNDS; RHODIUM; STOICHIOMETRY;

EID: 53049083816     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801460w     Document Type: Article
Times cited : (47)

References (50)
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    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 397
    • O'Neill, B.T.1
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    • Review: a
    • Review: (a) Dieter, R. K. Tetrahedron 1999, 55, 4177.
    • (1999) Tetrahedron , vol.55 , pp. 4177
    • Dieter, R.K.1
  • 19
    • 0842264108 scopus 로고    scopus 로고
    • Reaction of organozinc reagents with acid chlorides: (b) Kazmierski, I.; Bastienne, M.; Gosmini, C.; Paris, J. M.; Périchon, J. J. Org. Chem. 2004, 69, 936.
    • Reaction of organozinc reagents with acid chlorides: (b) Kazmierski, I.; Bastienne, M.; Gosmini, C.; Paris, J. M.; Périchon, J. J. Org. Chem. 2004, 69, 936.
  • 20
    • 33846031566 scopus 로고    scopus 로고
    • Reaction of organocopper reagents with acid chlorides; (c) Lin, W.; Baron, O.; Knochel, P. Org. Lett. 2006, 8, 5673.
    • Reaction of organocopper reagents with acid chlorides; (c) Lin, W.; Baron, O.; Knochel, P. Org. Lett. 2006, 8, 5673.
  • 21
    • 0033574716 scopus 로고    scopus 로고
    • Reactions of arylboronic acids with acid chlorides or acid anhydrides: (d) Haddach, M.; McCarthy, J. R. Tetrahedron Lett. 1999, 40, 3109.
    • Reactions of arylboronic acids with acid chlorides or acid anhydrides: (d) Haddach, M.; McCarthy, J. R. Tetrahedron Lett. 1999, 40, 3109.
  • 27
    • 0034669524 scopus 로고    scopus 로고
    • Reactions of arylboronic acids with thioesters: (j) Liebeskind, L.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260.
    • Reactions of arylboronic acids with thioesters: (j) Liebeskind, L.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260.
  • 36
    • 33750925523 scopus 로고    scopus 로고
    • For other approaches for the preparation of benzophenones from aldehydes, see; a
    • For other approaches for the preparation of benzophenones from aldehydes, see; (a) Crawford, J. J.; Henderson, K. W.; Kerr, W. J. Org. Lett. 2006, 8, 5073.
    • (2006) Org. Lett , vol.8 , pp. 5073
    • Crawford, J.J.1    Henderson, K.W.2    Kerr, W.J.3
  • 39
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    • For a discussion on the available approaches for the synthesis of sterically hindered benzophenones, see: (a) Hollinshead, S. P, Nichols, J. B, Wilson, J. W. J. Org. Chem. 1994, 59, 6703
    • For a discussion on the available approaches for the synthesis of sterically hindered benzophenones, see: (a) Hollinshead, S. P.; Nichols, J. B.; Wilson, J. W. J. Org. Chem. 1994, 59, 6703.
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    • 3K, see: (a) Navarre, L.; Darses, S.; Genet, J.-P. Angew. Chem., Int. Ed. 2004, 43, 719.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.