메뉴 건너뛰기




Volumn 39, Issue 4, 2009, Pages 613-625

Microwave-assisted K-10 montmorillonite clay-mediated knoevenagel hetero-Diels-Alder reactions: A novel protocol for the synthesis of polycyclic pyrano[2,3,4-kl]xanthene derivatives

Author keywords

1,3 Dione; Hetero Diels Alder reaction; Microwave; Pyrano xanthene

Indexed keywords

5,11A,15B 3 METHYL 1 PHENYLPYRAZOLO[3,2 C] 5,11A,12,13,14,15B OCTAHYDRO 1H PYRANO[2,3,4 KL]XANTHENE; 5,11A,15B INDAN 1 ONE[3,2 C] 5,11A,12,13,14,15B OCTAHYDRO 1H PYRANO[2,3,4 KL]XANTHENE; MONTMORILLONITE; UNCLASSIFIED DRUG; XANTHENE DERIVATIVE;

EID: 61849175896     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802417825     Document Type: Article
Times cited : (19)

References (20)
  • 1
    • 0000048482 scopus 로고
    • For reviews on the intramolecular Diels-Alder reaction, see (a, B. M. Trost, I. Fleming Eds, Pergamon: Oxford, UK, chapter 4.4, pp
    • For reviews on the intramolecular Diels-Alder reaction, see (a) Roush, W. R. In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming (Eds.); Pergamon: Oxford, UK, 1991; vol. 5, chapter 4.4, pp. 513-550;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 2
    • 0032838140 scopus 로고    scopus 로고
    • Harvesting Diels and Alder's garden: Synthetic investigations of intramolecular [4+2] cycloadditions
    • (b) Fallis, A. Harvesting Diels and Alder's garden: Synthetic investigations of intramolecular [4+2] cycloadditions. Acc. Chem. Res. 1999, 32, 464.
    • (1999) Acc. Chem. Res , vol.32 , pp. 464
    • Fallis, A.1
  • 3
    • 33947486579 scopus 로고
    • A study of the intramolecular Diels-Alder reaction
    • (a) House, H. O.; Cronin, T. H. A study of the intramolecular Diels-Alder reaction. J. Org. Chem. 1965, 30, 1061;
    • (1965) J. Org. Chem , vol.30 , pp. 1061
    • House, H.O.1    Cronin, T.H.2
  • 4
    • 0017803458 scopus 로고
    • Total synthesis of (±)-dendrobine
    • (b) Roush, W. R. Total synthesis of (±)-dendrobine. J. Am. Chem. Soc. 1978, 100, 3599;
    • (1978) J. Am. Chem. Soc , vol.100 , pp. 3599
    • Roush, W.R.1
  • 5
    • 0001588214 scopus 로고
    • Intramolecular Diels-Alder reactions: The angularly methylated trans-perhydroindan ring system
    • (c) Roush, W. R.; Peseckis, S. M. Intramolecular Diels-Alder reactions: The angularly methylated trans-perhydroindan ring system. J. Am. Chem. Soc. 1981, 103, 6696;
    • (1981) J. Am. Chem. Soc , vol.103 , pp. 6696
    • Roush, W.R.1    Peseckis, S.M.2
  • 6
    • 0005841830 scopus 로고
    • Lewis acid-catalysed intramolecular Diels-Alder cycloadditions: A mild method for the synthesis of bicyclo [n.3.1] bridgehead alkenes
    • (d) Shea, K. J.; Gilman, J. W. Lewis acid-catalysed intramolecular Diels-Alder cycloadditions: A mild method for the synthesis of bicyclo [n.3.1] bridgehead alkenes. Tetrahedron Lett. 1983, 24, 657.
    • (1983) Tetrahedron Lett , vol.24 , pp. 657
    • Shea, K.J.1    Gilman, J.W.2
  • 7
    • 0029491556 scopus 로고
    • Photophysical and photochemical properties of dye molecules in polymers used for fluorescent solar concentrators
    • Ion, R. M.; Fara, V. L. Photophysical and photochemical properties of dye molecules in polymers used for fluorescent solar concentrators. Proc. Indian Acad. Sci. 1995, 107, 825.
    • (1995) Proc. Indian Acad. Sci , vol.107 , pp. 825
    • Ion, R.M.1    Fara, V.L.2
  • 9
    • 17144387077 scopus 로고    scopus 로고
    • A photosensitization or a photocatalytic process
    • Ion, R. M. PDT - A photosensitization or a photocatalytic process. Prog. Catal. 1997, 2, 55.
    • (1997) Prog. Catal , vol.2 , pp. 55
    • Ion, R.M.P.1
  • 10
    • 0032253115 scopus 로고    scopus 로고
    • The incorporation of various porphyrins into blood cells measured via flow cytometry, absorption, and emission spectroscopy
    • Ion, R. M.; Frackowiak, D.; Plannar, A.; Wiktorowicz, K. The incorporation of various porphyrins into blood cells measured via flow cytometry, absorption, and emission spectroscopy. Acta Biochim. Pol. 1998, 45, 833.
    • (1998) Acta Biochim. Pol , vol.45 , pp. 833
    • Ion, R.M.1    Frackowiak, D.2    Plannar, A.3    Wiktorowicz, K.4
  • 11
    • 27744579044 scopus 로고
    • 1]Benzopyrano[2,3-b]xanthene derivatives. Jpn. Tokkyo Koho JP 56005480, 27 June 1979
    • Hideu, T. [1]Benzopyrano[2,3-b]xanthene derivatives. Jpn. Tokkyo Koho JP 56005480, 27 June 1979; Chem. Abstr. 1981, 95, 80922b.
    • (1981) Chem. Abstr , vol.95
    • Hideu, T.1
  • 12
    • 27744488727 scopus 로고    scopus 로고
    • Preparation of pyrimidine nucleosides as thymidine kinase inhibitors and virucides
    • PCT Int. Appl. WO 9706178, P212377y
    • Lamberk, R. W.; Martin, J. A.; Merrett, J. H.; Parkes, K. E. B.; Thomas, G. J. Preparation of pyrimidine nucleosides as thymidine kinase inhibitors and virucides. PCT Int. Appl. WO 9706178, 1997; Chem. Abstr. 1997, 126, P212377y.
    • (1997) Chem. Abstr , vol.126
    • Lamberk, R.W.1    Martin, J.A.2    Merrett, J.H.3    Parkes, K.E.B.4    Thomas, G.J.5
  • 14
    • 33846338767 scopus 로고    scopus 로고
    • Rathna Durga, R.; Jayashankaran, J.; Raghunathan, R. A rapid access to indolo[2,1-a]pyrrolo[4′,3′:4,5]pyrano[5,6-c]coumarin/ [6,5-c]chromone derivatives by domino Knoevenagal intramolecular hetero-Diels-Alder reactions. Tetrahedron Lett. 2007, 48, 1385-1389.
    • Rathna Durga, R.; Jayashankaran, J.; Raghunathan, R. A rapid access to indolo[2,1-a]pyrrolo[4′,3′:4,5]pyrano[5,6-c]coumarin/ [6,5-c]chromone derivatives by domino Knoevenagal intramolecular hetero-Diels-Alder reactions. Tetrahedron Lett. 2007, 48, 1385-1389.
  • 15
    • 33344474176 scopus 로고    scopus 로고
    • An efficient synthesis of thiopyrano[5,6-c]coumarin/[6,5-c]chromones through intramolecular domino Knoevenagel hetero-Diels-Alder reactions
    • Jayashankaran, J.; Rathna Durga, R.; Raghunathan, R. An efficient synthesis of thiopyrano[5,6-c]coumarin/[6,5-c]chromones through intramolecular domino Knoevenagel hetero-Diels-Alder reactions. Tetrahedron Lett. 2006, 47, 2265-2270.
    • (2006) Tetrahedron Lett , vol.47 , pp. 2265-2270
    • Jayashankaran, J.1    Rathna Durga, R.2    Raghunathan, R.3
  • 16
    • 37849016138 scopus 로고    scopus 로고
    • Sugi Kamala, E. T.; Nirmala, S.; Sudha, L.; Ramesh, E.; Raghunathan, R. Actacis-3-methyl-1-phenyl-8a,9,10,11,12,12a,12b-hexahydro-1H, 3bH-pyrazolo[ 3,4:2′,3′]pyrano[4′,5′,6′- kl]xanthene. Cryst. E Acta Cryst. 2008, E64, o245-o246.
    • Sugi Kamala, E. T.; Nirmala, S.; Sudha, L.; Ramesh, E.; Raghunathan, R. Actacis-3-methyl-1-phenyl-8a,9,10,11,12,12a,12b-hexahydro-1H, 3bH-pyrazolo[ 3,4:2′,3′]pyrano[4′,5′,6′- kl]xanthene. Cryst. E Acta Cryst. 2008, E64, o245-o246.
  • 17
    • 33846818691 scopus 로고    scopus 로고
    • Solvent-free microwave-assisted conversion of Baylis-Hillman adducts of ninhydrin into functionalized spiropyrrolidines/pyrrolizidines through 1,3-dipolar cycloaddition
    • Ramesh, E.; Kathiresan, M.; Raghunathan, R. Solvent-free microwave-assisted conversion of Baylis-Hillman adducts of ninhydrin into functionalized spiropyrrolidines/pyrrolizidines through 1,3-dipolar cycloaddition. Tetrahedron Lett. 2007, 48, 1835-1839.
    • (2007) Tetrahedron Lett , vol.48 , pp. 1835-1839
    • Ramesh, E.1    Kathiresan, M.2    Raghunathan, R.3
  • 18
    • 4444356117 scopus 로고    scopus 로고
    • A facile synthesis of novel dispiroheterocycles through solvent-free microwave-assisted [3+2] cycloaddition of azomethine ylides
    • Jayashankaran, J.; Rathna Durga R. S., Manian; Raghunathan, R. A facile synthesis of novel dispiroheterocycles through solvent-free microwave-assisted [3+2] cycloaddition of azomethine ylides. Tetrahedron Lett. 2004, 45, 7303-7305.
    • (2004) Tetrahedron Lett , vol.45 , pp. 7303-7305
    • Jayashankaran, J.1    Rathna Durga, R.S.2    Manian3    Raghunathan, R.4
  • 19
    • 19044399555 scopus 로고    scopus 로고
    • A regioselective synthesis of dispiro[oxindole-cyclohexanone]pyrrolidines and dispiro[oxindole-hexahydroindazole]pyrrolidines by sequential 1,3-dipolar cycloaddition and annulation through a microwave induced solvent-free approach
    • Jayashankaran, J.; Rathna Durga R. S., Manian; Raghunathan, R. A regioselective synthesis of dispiro[oxindole-cyclohexanone]pyrrolidines and dispiro[oxindole-hexahydroindazole]pyrrolidines by sequential 1,3-dipolar cycloaddition and annulation through a microwave induced solvent-free approach. Tetrahedron 2005, 61, 5595-5598.
    • (2005) Tetrahedron , vol.61 , pp. 5595-5598
    • Jayashankaran, J.1    Rathna Durga, R.S.2    Manian3    Raghunathan, R.4
  • 20
    • 84985611212 scopus 로고
    • Control of the conformation of transition states in intramolecular Diels-Alder reactions with inverse electron demand
    • Tietze, L. F.; Stegelmeier, H.; Harms, K.; Brumby, T. Control of the conformation of transition states in intramolecular Diels-Alder reactions with inverse electron demand. Angew. Chem. Int. Ed. 1982, 21, 863.
    • (1982) Angew. Chem. Int. Ed , vol.21 , pp. 863
    • Tietze, L.F.1    Stegelmeier, H.2    Harms, K.3    Brumby, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.