메뉴 건너뛰기




Volumn 46, Issue 29, 2007, Pages 5559-5561

Ruthenium hydride catalyzed regioselective addition of aldehydes to enones to give 1,3-diketones

Author keywords

Addition; Aldehydes; Enones; Homogeneous catalysis; Ruthenium

Indexed keywords

ADDITION REACTIONS; KETONES; REGIOSELECTIVITY; RUTHENIUM;

EID: 34547183280     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200701005     Document Type: Article
Times cited : (70)

References (34)
  • 3
    • 30944445644 scopus 로고    scopus 로고
    • For recent work on the preparation of 1,3-diketones, see a
    • For recent work on the preparation of 1,3-diketones, see a) S. Kamijo, G. B. Dudley, Org. Lett. 2006, 8, 175;
    • (2006) Org. Lett , vol.8 , pp. 175
    • Kamijo, S.1    Dudley, G.B.2
  • 9
  • 10
    • 0000017202 scopus 로고
    • see also the original work: g
    • see also the original work: g) G. Stork, R. Terrell, J. Am. Chem. Soc. 1954, 76, 2029.
    • (1954) J. Am. Chem. Soc , vol.76 , pp. 2029
    • Stork, G.1    Terrell, R.2
  • 11
    • 30744478964 scopus 로고    scopus 로고
    • For recent methods for preparing 2-alkyl-substituted 1,3-diketones based on the catalytic alkylation of 1,3-diketones, see a
    • For recent methods for preparing 2-alkyl-substituted 1,3-diketones based on the catalytic alkylation of 1,3-diketones, see a) Z. Li, C. J. Li, J. Am. Chem. Soc. 2006, 128, 56;
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 56
    • Li, Z.1    Li, C.J.2
  • 15
    • 0035930763 scopus 로고    scopus 로고
    • For examples of transition-metal-catalyzed hydroacylation of enones leading to 1,4-diketones, see a M. C. Willis, S. Sapmaz, Chem. Commun. 2001, 2558;
    • For examples of transition-metal-catalyzed hydroacylation of enones leading to 1,4-diketones, see a) M. C. Willis, S. Sapmaz, Chem. Commun. 2001, 2558;
  • 17
    • 33646923706 scopus 로고    scopus 로고
    • For our previous work on the use of the ruthenium hydride catalyst, see a
    • For our previous work on the use of the ruthenium hydride catalyst, see a) T. Doi, T. Fukuyama, S. Minamino, G. Husson, I. Ryu, Chem. Commun. 2006, 1875;
    • (2006) Chem. Commun , pp. 1875
    • Doi, T.1    Fukuyama, T.2    Minamino, S.3    Husson, G.4    Ryu, I.5
  • 21
    • 0000324975 scopus 로고    scopus 로고
    • Using a similar system comprising α,β-unsaturated ketones, aldehydes, and [RuH2(PPh3)4] under neat conditions, a Morita-Baylis, Hillman-type reaction was reported to take place, with PPh3 playing a role, see S. Sato, I. Matsuda, M. Shibata, J. Organomet. Chem. 1989, 377, 347
    • 3 playing a role, see S. Sato, I. Matsuda, M. Shibata, J. Organomet. Chem. 1989, 377, 347.
  • 22
    • 33744469835 scopus 로고    scopus 로고
    • 3 and p-nitrophenol, see M. Shi, Y.-H. Liu, Org. Biomol. Chem. 2006, 4, 1468.
    • 3 and p-nitrophenol, see M. Shi, Y.-H. Liu, Org. Biomol. Chem. 2006, 4, 1468.
  • 23
    • 34547162545 scopus 로고    scopus 로고
    • We thank one of the referees for calling our attention to the mechanistic possibility in our system
    • We thank one of the referees for calling our attention to the mechanistic possibility in our system.
  • 27
    • 15844412400 scopus 로고    scopus 로고
    • For examples of catalytic transformations based on ruthenium enolates, see a S.-I. Murahashi, T. Naota, H. Taki, M. Mizuno, H. Takaya, S. Komiya, Y. Mizuho, N. Oyasato, M. Hiraoka, M. Hirano, A. Fukuoka, J. Am. Chem. Soc. 1995, 117, 12436;
    • For examples of catalytic transformations based on ruthenium enolates, see a) S.-I. Murahashi, T. Naota, H. Taki, M. Mizuno, H. Takaya, S. Komiya, Y. Mizuho, N. Oyasato, M. Hiraoka, M. Hirano, A. Fukuoka, J. Am. Chem. Soc. 1995, 117, 12436;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.