메뉴 건너뛰기




Volumn 53, Issue 37, 2012, Pages 4979-4983

Indium-mediated regioselective mono-allylation of 1,5-dicarbonyl compounds and dehydrative cyclization to 2,3-dihydro-4H-pyran-4-ones and 3,4-dihydro-2H-[1,4]oxazines

Author keywords

1,5 Dicarbonyl compounds; 2,3 Dihydro 4H pyran 4 ones; 3,4 Dihydro 2H 1,4 oxazines; Indium

Indexed keywords

1,4 OXAZINE DERIVATIVE; 1,5 DICARBONYL DERIVATIVE; 2,3 DIHYDRO 4H PYRAN 4 ONE; 3,4 DIHYDRO 2H[1,4]OXAZINE; 4 PYRONE DERIVATIVE; CARBONYL DERIVATIVE; INDIUM; UNCLASSIFIED DRUG;

EID: 84864979992     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.07.022     Document Type: Article
Times cited : (7)

References (81)
  • 6
    • 4544247886 scopus 로고    scopus 로고
    • For the synthesis of 2,3-dihydro-4H-pyran-4-ones by a hetero-Diels-Alder reaction, see: K.A. Jorgensen Eur. J. Org. Chem. 2004 2093 2102
    • (2004) Eur. J. Org. Chem. , pp. 2093-2102
    • Jorgensen, K.A.1
  • 12
    • 0742269535 scopus 로고    scopus 로고
    • For the synthesis of 2,3-dihydro-4H-pyran-4-ones via a cyclization of β-hydroxyenones, β-hydroxyynones, and related compounds see: M. Reiter, S. Ropp, and V. Gouverneur Org. Lett. 6 2004 91 94
    • (2004) Org. Lett. , vol.6 , pp. 91-94
    • Reiter, M.1    Ropp, S.2    Gouverneur, V.3
  • 18
    • 65449176745 scopus 로고    scopus 로고
    • For the synthesis of 2,3-dihydro-4H-pyran-4-ones via an acid-catalyzed cyclization of 5-hydroxy-1,3-diketones and related compounds see: R. Ahmad, R.A. Khera, A. Villinger, and P. Langer Tetrahedron Lett. 50 2009 3020 3022
    • (2009) Tetrahedron Lett. , vol.50 , pp. 3020-3022
    • Ahmad, R.1    Khera, R.A.2    Villinger, A.3    Langer, P.4
  • 28
    • 79960949651 scopus 로고    scopus 로고
    • For the synthesis of natural products bearing a 2,3-dihydro-4H-pyran-4- one moiety using an acid-catalyzed cyclization protocol of 5-hydroxy-1,3- diketones, see: K. Tsubone, K. Hashizume, H. Fuwa, and M. Sasaki Tetrahedron 67 2011 6600 6615
    • (2011) Tetrahedron , vol.67 , pp. 6600-6615
    • Tsubone, K.1    Hashizume, K.2    Fuwa, H.3    Sasaki, M.4
  • 53
  • 54
    • 70549111634 scopus 로고    scopus 로고
    • For the isolation and crystallographic characterization of allylindium species, see: M. Yasuda, M. Haga, and A. Baba Eur. J. Org. Chem. 2009 5513 5517
    • (2009) Eur. J. Org. Chem. , pp. 5513-5517
    • Yasuda, M.1    Haga, M.2    Baba, A.3
  • 74
    • 84857062120 scopus 로고    scopus 로고
    • For the selected examples on the oxonium-ene reaction, see: P. Saha, and A.K. Saikia Tetrahedron 68 2012 2261 2266
    • (2012) Tetrahedron , vol.68 , pp. 2261-2266
    • Saha, P.1    Saikia, A.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.