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Volumn 56, Issue 17, 2000, Pages 2709-2712

Trialkylamine controlled phenol-for maldehyde reaction over clay catalysts: Selective and environmentally benign synthesis of salicylic aldehydes

Author keywords

Clay; Heterogeneous catalysis; Salicylic aldehydes

Indexed keywords

ALDEHYDE; ALIPHATIC AMINE; FORMALDEHYDE; MONTMORILLONITE; PHENOL; SALICYLIC ACID DERIVATIVE;

EID: 0034697360     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00171-X     Document Type: Article
Times cited : (32)

References (41)
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    • The Knoevenagel Reaction
    • (d) Trost, B. M., Fleming, I., Heathcock, C. H., Eds.; Pergamon Press: Oxford
    • (d) Tietze, L. F.; Beifuss, U. The Knoevenagel Reaction. In Comprehensive Organic Synthesis, Trost, B. M., Fleming, I., Heathcock, C. H., Eds.; Pergamon Press: Oxford, 1991; Vol. 2, pp 341-394.
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    • Tietze, L.F.1    Beifuss, U.2
  • 6
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    • For the recent application of salen-type ligands see: (a)
    • For the recent application of salen-type ligands see: (a) Larrow, J. F.; Schaus, S. E.; Jacobsen, E. N. J. Am. Chem. Soc. 1996, 118, 7420.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7420
    • Larrow, J.F.1    Schaus, S.E.2    Jacobsen, E.N.3
  • 9
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    • (a) Eur. Pat. Appl. EP536,960 1993 (C.A. 1993, 119, 116962v)
    • (a) Shuttleworth, R.; Fielden, J. M.; Levin, D. Eur. Pat. Appl. EP536,960 1993 (C.A. 1993, 119, 116962v).
    • Shuttleworth, R.1    Fielden, J.M.2    Levin, D.3
  • 10
    • 0342451785 scopus 로고    scopus 로고
    • (b) Eur. Pat. Appl. EP529,870, 1993 (C.A. 1993, 119, 95098a)
    • (b) Levin, D. Eur. Pat. Appl. EP529,870, 1993 (C.A. 1993, 119, 95098a).
    • Levin, D.1
  • 16
  • 29
    • 0342886185 scopus 로고    scopus 로고
    • Conversion and yield were then estimated by GC analysis [SE-30 packed column, 1.5 m, 80°C (2), 10°C/min, 280°C (3)]
    • Conversion and yield were then estimated by GC analysis [SE-30 packed column, 1.5 m, 80°C (2), 10°C/min, 280°C (3)].
  • 30
    • 0032546309 scopus 로고    scopus 로고
    • Solid acid-promoted acetalisation of carbonyl compound with diols is well documented in the literature and references cited therein
    • Solid acid-promoted acetalisation of carbonyl compound with diols is well documented in the literature: Ballini, R.; Bosica, G.; Frullanti, B.; Maggi, R.; Sartori, G.; Schroer, F. Tetrahedron Lett. 1998, 38, 1615 and references cited therein.
    • (1998) Tetrahedron Lett. , vol.38 , pp. 1615
    • Ballini, R.1    Bosica, G.2    Frullanti, B.3    Maggi, R.4    Sartori, G.5    Schroer, F.6
  • 33
    • 0031048486 scopus 로고    scopus 로고
    • Meerwein-Ponndorf-Verley and Oppenhauer reactions under solid acid or basic catalysis were recently reported; see for example (a)
    • Meerwein-Ponndorf-Verley and Oppenhauer reactions under solid acid or basic catalysis were recently reported; see for example (a) Creyghton, E. J.; Ganeshie, S. D.; Downing, R. S.; van Bekkum, H. J. Mol. Catal. A 1997, 115, 457.
    • (1997) J. Mol. Catal. A , vol.115 , pp. 457
    • Creyghton, E.J.1    Ganeshie, S.D.2    Downing, R.S.3    Van Bekkum, H.4
  • 36
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    • 2O (1.9%)
    • 2O (1.9%).
  • 37
    • 0342886183 scopus 로고    scopus 로고
    • 3N, respectively
    • 3N, respectively.
  • 38
    • 0002431582 scopus 로고
    • The OH-promoted ortho-regioselective alkylation of phenol substrates with formaldehyde is well documented in the literature: (a)
    • The OH-promoted ortho-regioselective alkylation of phenol substrates with formaldehyde is well documented in the literature: (a) Casiraghi, G.; Casnati, G.; Puglia, G.; Sartori, G. Synthesis 1980, 124.
    • (1980) Synthesis , pp. 124
    • Casiraghi, G.1    Casnati, G.2    Puglia, G.3    Sartori, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.