메뉴 건너뛰기




Volumn 37, Issue 10, 2007, Pages 1659-1664

Cation-exchanged resins: Efficient heterogeneous catalysts for facile synthesis of 1-amidoalkyl-2-naphthols from one-pot, three-component condensations of amides/ureas, aldehydes, and 2-naphthol

Author keywords

1 amidoalkyl 2 naphthols; Cation exchange resins; Indion 130; Multicomponent reaction

Indexed keywords

2 NAPHTHOL; ALDEHYDE DERIVATIVE; AMIDE; NAPHTHOL DERIVATIVE; UREA DERIVATIVE;

EID: 34249276057     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910701263858     Document Type: Article
Times cited : (113)

References (21)
  • 1
    • 2542509173 scopus 로고    scopus 로고
    • Multicomponent reactions with isocyanides
    • (a) Domling, A.; Ugi, I. Multicomponent reactions with isocyanides. Angew. Chem. Int. Ed. 2000, 39, 3168-3210;
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 3168-3210
    • Domling, A.1    Ugi, I.2
  • 2
    • 7044263277 scopus 로고    scopus 로고
    • Synthesis and application of small molecule libraries
    • (b) Thomson, L. A.; Ellman, J. A. Synthesis and application of small molecule libraries. Chem. Rev. 1996, 96, 555-600.
    • (1996) Chem. Rev , vol.96 , pp. 555-600
    • Thomson, L.A.1    Ellman, J.A.2
  • 3
  • 4
    • 0001300841 scopus 로고
    • The Mannich reaction
    • Robert, E, Ed, Krieger: New York
    • (b) Blicke, F. F. The Mannich reaction. Org. React. Coll; Robert, E., Ed.; Krieger: New York, 1942; Vol. I, p. 303.
    • (1942) Org. React. Coll , vol.1 , pp. 303
    • Blicke, F.F.1
  • 5
    • 85067856671 scopus 로고
    • Advances in the chemistry of Mannich bases
    • (a) Tramontini, M. Advances in the chemistry of Mannich bases. Synthesis 1973, 12, 703-775;
    • (1973) Synthesis , vol.12 , pp. 703-775
    • Tramontini, M.1
  • 6
    • 0014284128 scopus 로고
    • The Mannich reaction: Mechanistic and technological considerations
    • (b) Thompson, B. B. The Mannich reaction: mechanistic and technological considerations. J. Pharm. Sci. 1968, 57, 715-733;
    • (1968) J. Pharm. Sci , vol.57 , pp. 715-733
    • Thompson, B.B.1
  • 7
    • 0036273273 scopus 로고    scopus 로고
    • Linked Pummerer-Mannich ion cyclizations for heterocyclic chemistry
    • (c) Padwa, A.; Bur, S. K.; Danca, D. M.; Ginn, J. D.; Lynch, S. M. Linked Pummerer-Mannich ion cyclizations for heterocyclic chemistry. Synlett 2002, 6, 851-862.
    • (2002) Synlett , vol.6 , pp. 851-862
    • Padwa, A.1    Bur, S.K.2    Danca, D.M.3    Ginn, J.D.4    Lynch, S.M.5
  • 8
    • 0001642827 scopus 로고
    • Quinone methides: Base-catalyzed condensation reactions of hydroxybenzyl alcohols and ethers
    • Merijan, A.; Gardner, P. D. Quinone methides: Base-catalyzed condensation reactions of hydroxybenzyl alcohols and ethers. J. Org. Chem. 1965, 30, 3965-3967;
    • (1965) J. Org. Chem , vol.30 , pp. 3965-3967
    • Merijan, A.1    Gardner, P.D.2
  • 9
    • 30744455580 scopus 로고
    • Reaction of phenolic Mannich base methiodides and oxides with various nucleophiles
    • (b) Gardner, P. D.; Rafsanjani, H. S.; Rand, L. Reaction of phenolic Mannich base methiodides and oxides with various nucleophiles. J. Am. Chem. Soc. 1959, 51, 3364-3367;
    • (1959) J. Am. Chem. Soc , vol.51 , pp. 3364-3367
    • Gardner, P.D.1    Rafsanjani, H.S.2    Rand, L.3
  • 10
    • 0030833252 scopus 로고    scopus 로고
    • Synthesis and chemistry of quinone methide models for the anthracycline antitumor antibiotics
    • (c) Angle, S. R.; Rainer, J. D.; Woytowiez, Z. Synthesis and chemistry of quinone methide models for the anthracycline antitumor antibiotics. J. Org. Chem. 1997, 62, 5884-5892;
    • (1997) J. Org. Chem , vol.62 , pp. 5884-5892
    • Angle, S.R.1    Rainer, J.D.2    Woytowiez, Z.3
  • 11
    • 8744281396 scopus 로고    scopus 로고
    • A 2:1 coupling reaction of arynes with aldehydes via o-quinone methides: Straightforward synthesis of 9-arylxanthenes
    • (d) Yoshida, H.; Watanabe, M.; Fukushima, H.; Ohshita, J.; Kunai, A. A 2:1 coupling reaction of arynes with aldehydes via o-quinone methides: straightforward synthesis of 9-arylxanthenes. Org. Lett. 2004, 6, 4049-4051.
    • (2004) Org. Lett , vol.6 , pp. 4049-4051
    • Yoshida, H.1    Watanabe, M.2    Fukushima, H.3    Ohshita, J.4    Kunai, A.5
  • 12
    • 33645763534 scopus 로고    scopus 로고
    • A simple and efficient procedure for the synthesis of amidoalkyl naphthols by p-TSA in solution or under solvent-free condition
    • (a) Khodaei, M. M.; Khosropour, A. R.; Moghanian, H. A simple and efficient procedure for the synthesis of amidoalkyl naphthols by p-TSA in solution or under solvent-free condition. Synlett 2006, 6, 916-920;
    • (2006) Synlett , vol.6 , pp. 916-920
    • Khodaei, M.M.1    Khosropour, A.R.2    Moghanian, H.3
  • 13
    • 17144400729 scopus 로고    scopus 로고
    • Simple and convenient method for the synthesis of 14-alkyl or aryl-14-H- dibenzo[a, j]xanthenes catalyzed by p-TSA in solution and solvent-free conditions
    • (b) Khodaei, M. M.; Khosropour, A. R.; Moghanian, H. A Facile. Simple and convenient method for the synthesis of 14-alkyl or aryl-14-H- dibenzo[a, j]xanthenes catalyzed by p-TSA in solution and solvent-free conditions. Synlett 2005, 6, 955-958.
    • (2005) Synlett , vol.6 , pp. 955-958
    • Khodaei, M.M.1    Khosropour, A.R.2    Moghanian, H.3    Facile, A.4
  • 14
    • 0033722687 scopus 로고    scopus 로고
    • Incorporation of gallium into zeolites: Synthesis, properties and catalytic application
    • (a) Fricke, R.; Hosslick, H.; Lischke, G.; Richter, M. Incorporation of gallium into zeolites: synthesis, properties and catalytic application. Chem. Rev. 2000, 100, 2303-2405;
    • (2000) Chem. Rev , vol.100 , pp. 2303-2405
    • Fricke, R.1    Hosslick, H.2    Lischke, G.3    Richter, M.4
  • 15
    • 85031221315 scopus 로고
    • Molding clays into efficient catalysts
    • (b) Andre, C.; Pierre, L. Molding clays into efficient catalysts. Synlett 1994, 3, 155-161.
    • (1994) Synlett , vol.3 , pp. 155-161
    • Andre, C.1    Pierre, L.2
  • 16
    • 20444414513 scopus 로고    scopus 로고
    • A simple and greener protocol for the preparation of β-acetylamino ketones by a one-pot reaction of aryl aldehydes, enolisable ketones, acetyl chloride and acetonitrile in the presence of zeolite Hβ as a reusable catalyst
    • (a) Bhat, R. P.; Raje, V. P.; Alexander, V. M.; Patil, S. B.; Samant, S. D. A simple and greener protocol for the preparation of β-acetylamino ketones by a one-pot reaction of aryl aldehydes, enolisable ketones, acetyl chloride and acetonitrile in the presence of zeolite Hβ as a reusable catalyst. Tetrahedron Lett. 2005, 4801-4803;
    • (2005) Tetrahedron Lett , pp. 4801-4803
    • Bhat, R.P.1    Raje, V.P.2    Alexander, V.M.3    Patil, S.B.4    Samant, S.D.5
  • 17
    • 11844304986 scopus 로고    scopus 로고
    • One-pot synthesis of N-substituted (3-oxobutanyl)carbamates from primary amines using modified zeolite Hβ at room temperature
    • (b) Raje, V. P.; Bhat, R. P.; Samant, S. D. One-pot synthesis of N-substituted (3-oxobutanyl)carbamates from primary amines using modified zeolite Hβ at room temperature. Tetrahedron Lett. 2005, 46, 835-837;
    • (2005) Tetrahedron Lett , vol.46 , pp. 835-837
    • Raje, V.P.1    Bhat, R.P.2    Samant, S.D.3
  • 18
    • 13244256989 scopus 로고    scopus 로고
    • Amberlyst-15® as a novel and recyclable solid acid for the coupling of aromatic aldehydes with homopropargyl alcohol
    • (c) Yadav, J. S.; Reddy, B. V. S.; Vishnumurthy, P. Amberlyst-15® as a novel and recyclable solid acid for the coupling of aromatic aldehydes with homopropargyl alcohol. Tetrahedron Lett. 2005, 46, 1311-1313;
    • (2005) Tetrahedron Lett , vol.46 , pp. 1311-1313
    • Yadav, J.S.1    Reddy, B.V.S.2    Vishnumurthy, P.3
  • 19
    • 11144267793 scopus 로고    scopus 로고
    • Amberlyst-15®-promoted efficient 2-halogenation of 1,3-keto-esters and cyclic ketones using N-halosuccinimides
    • (d) Meshram, H. M.; Reddy, P. N.; Sadashiv, K.; Yadav, J. S. Amberlyst-15®-promoted efficient 2-halogenation of 1,3-keto-esters and cyclic ketones using N-halosuccinimides. Tetrahedron Lett. 2005, 46, 623-626.
    • (2005) Tetrahedron Lett , vol.46 , pp. 623-626
    • Meshram, H.M.1    Reddy, P.N.2    Sadashiv, K.3    Yadav, J.S.4
  • 20
    • 0029369457 scopus 로고
    • Some novel aspects of cationic ion-exchanged resins as catalysts
    • (a) Sharma, M. M. Some novel aspects of cationic ion-exchanged resins as catalysts. React. Funct. Polym. 1995, 26, 3-23;
    • (1995) React. Funct. Polym , vol.26 , pp. 3-23
    • Sharma, M.M.1
  • 21
    • 0027625438 scopus 로고
    • Cationic ion exchange resins as catalyst
    • (b) Chakrabarti, A.; Sharma, M. M. Cationic ion exchange resins as catalyst. React. Polym. 1993, 20, 1-45.
    • (1993) React. Polym , vol.20 , pp. 1-45
    • Chakrabarti, A.1    Sharma, M.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.