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Volumn 8, Issue 24, 2006, Pages 5657-5660

Reductive aldol coupling of divinyl ketones via rhodium-catalyzed hydrogenation: Syn-diastereoselective construction of β-hydroxyenones

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CATION; KETONE; RHODIUM; VINYL DERIVATIVE;

EID: 33845976661     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0624023     Document Type: Article
Times cited : (39)

References (45)
  • 1
    • 0000191874 scopus 로고
    • For rhodium-catalyzed reductive aldol reaction mediated by silane or other reductants, see: a
    • For rhodium-catalyzed reductive aldol reaction mediated by silane or other reductants, see: (a) Revis, A.; Hilty, T. K. Tetrahedron Lett. 1987, 28, 4809-4812.
    • (1987) Tetrahedron Lett , vol.28 , pp. 4809-4812
    • Revis, A.1    Hilty, T.K.2
  • 10
    • 0037176242 scopus 로고    scopus 로고
    • For rhodium-catalyzed reductive aldol reaction mediated by hydrogen, see: a
    • For rhodium-catalyzed reductive aldol reaction mediated by hydrogen, see: (a) Jang, H.-Y.; Huddleston, R. R.; Krische, M. J. J. Am. Chem. Soc. 2002, 124, 15156-15157.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 15156-15157
    • Jang, H.-Y.1    Huddleston, R.R.2    Krische, M.J.3
  • 15
    • 0001899091 scopus 로고
    • For cobalt-catalyzed reductive aldol reaction, see: a
    • For cobalt-catalyzed reductive aldol reaction, see: (a) Isayama, S.; Mukaiyama, T. Chem. Lett. 1989, 2005-2008.
    • (1989) Chem. Lett , pp. 2005-2008
    • Isayama, S.1    Mukaiyama, T.2
  • 19
    • 0001494417 scopus 로고    scopus 로고
    • For reductive aldol coupling catalyzed by other metals, see the following. Iridium: (a) Zhao, C.-X.; Duffey, M. O.; Taylor, S. J.; Morken, J. P. Org. Lett. 2001, 3, 1829-1831.
    • For reductive aldol coupling catalyzed by other metals, see the following. Iridium: (a) Zhao, C.-X.; Duffey, M. O.; Taylor, S. J.; Morken, J. P. Org. Lett. 2001, 3, 1829-1831.
  • 28
    • 0000131734 scopus 로고
    • For tri-2-furylphosphine effects in metal-catalyzed reactions, see: a
    • For tri-2-furylphosphine effects in metal-catalyzed reactions, see: (a) Farina, V.; Krishnan, B. J. Am. Chem. Soc. 1991, 113, 9585-9595.
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 9585-9595
    • Farina, V.1    Krishnan, B.2
  • 31
    • 20944436033 scopus 로고    scopus 로고
    • To date, a single study of catalyzed aldol additions involving aldol donors incorporating an enone moiety has been reported: Trost, B. M.; Shin, S.; Sclafani, J. A. J. Am. Chem. Soc. 2005, 127, 8602-8603.
    • To date, a single study of catalyzed aldol additions involving aldol donors incorporating an enone moiety has been reported: Trost, B. M.; Shin, S.; Sclafani, J. A. J. Am. Chem. Soc. 2005, 127, 8602-8603.
  • 32
    • 0025239937 scopus 로고
    • For noncatalyzed aldol additions of preformed enolates derived from methyl enones, see: a
    • For noncatalyzed aldol additions of preformed enolates derived from methyl enones, see: (a) Patterson, I.; Osborne, S. Tetrahedron Lett. 1990, 31, 2213-2216.
    • (1990) Tetrahedron Lett , vol.31 , pp. 2213-2216
    • Patterson, I.1    Osborne, S.2
  • 37
    • 33846017765 scopus 로고    scopus 로고
    • Enones constrained in the s-trans configuration, such as cyclohexenone, do not participate in hydrogen-mediated reductive aldol coupling
    • Enones constrained in the s-trans configuration, such as cyclohexenone, do not participate in hydrogen-mediated reductive aldol coupling.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.