메뉴 건너뛰기




Volumn 13, Issue 1, 2007, Pages 35-41

Synthesis of dibenzylidene sorbitol series compound

Author keywords

Acetal derivatives; Alditol; Sorbitol; Substituted benzaldehyde

Indexed keywords

ACYLATION; CATALYST ACTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NUCLEAR MAGNETIC RESONANCE; REACTION KINETICS;

EID: 34247380379     PISSN: 10064982     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (20)
  • 1
    • 34247337583 scopus 로고
    • Manufacture of benzylidene sorbitols
    • US: 3721682, 1973-03-20
    • Murai K, Akazome G, Choshi Y et al. Manufacture of Benzylidene Sorbitols [P]. US: 3721682, 1973-03-20.
    • (1973)
    • Murai, K.1    Akazome, G.2    Choshi, Y.3
  • 2
    • 34247338812 scopus 로고
    • Process for preparing dibenzylidene sorbitol and composition containing the same
    • US: 4267110, 1981-03-12
    • Uchiyama H. Process for Preparing Dibenzylidene Sorbitol and Composition Containing the Same [P]. US: 4267110, 1981-03-12.
    • (1981)
    • Uchiyama, H.1
  • 3
    • 34247398225 scopus 로고
    • Polyolefin resin composition comprising a dibenzylidene sorbitol derivative
    • US: 4483952, 1984-11-20
    • Uchiyama H. Polyolefin Resin Composition Comprising a Dibenzylidene Sorbitol Derivative [P]. US: 4483952, 1984-11-20.
    • (1984)
    • Uchiyama, H.1
  • 4
    • 34247387878 scopus 로고
    • Preparation of acetal
    • US: 4459418, 1984-07-10
    • James N G. Preparation of Acetal [P]. US: 4459418, 1984-07-10.
    • (1984)
    • James, N.G.1
  • 5
    • 34247336218 scopus 로고
    • Process for preparing dibenzylidene sorbitols and dibenzyldene xylitols
    • US: 4429140, 1984-01-31
    • Murai K, Kobayashi T, Fujitani K. Process for Preparing Dibenzylidene Sorbitols and Dibenzyldene Xylitols [P]. US: 4429140, 1984-01-31.
    • (1984)
    • Murai, K.1    Kobayashi, T.2    Fujitani, K.3
  • 6
    • 34247335774 scopus 로고
    • Method for producing a di-acetal of sorbitol and an aromatic aldehyde
    • US: 4562265, 1985-12-31
    • Machell G. Method for Producing a Di-acetal of Sorbitol and an Aromatic Aldehyde [P]. US: 4562265, 1985-12-31.
    • (1985)
    • Machell, G.1
  • 7
    • 34247346443 scopus 로고
    • Process for batchwise acetal production
    • US: 4902807, 1990-02-20
    • Kobayashi T, Kujitani K. Process for Batchwise Acetal Production [P]. US: 4902807, 1990-02-20.
    • (1990)
    • Kobayashi, T.1    Kujitani, K.2
  • 8
    • 34247364377 scopus 로고    scopus 로고
    • Method of making acetals
    • US: 5371474, 1998-03-24
    • Walter A S, Joseph M S. Method of Making Acetals [P]. US: 5371474, 1998-03-24.
    • (1998)
    • Walter, A.S.1    Joseph, M.S.2
  • 9
    • 34247392345 scopus 로고
    • Process for preparation of diacetal compounds
    • US: 5120863, 1992-01-09
    • Kobayashi T. Process for Preparation of Diacetal Compounds [P]. US: 5120863, 1992-01-09.
    • (1992)
    • Kobayashi, T.1
  • 10
    • 34247403337 scopus 로고
    • Process for purifying crude dibenzylidene sorbitol
    • US: 4131612, 1978-12-26
    • Uchiyama H. Process for Purifying Crude Dibenzylidene Sorbitol [P]. US: 4131612, 1978-12-26.
    • (1978)
    • Uchiyama, H.1
  • 11
    • 34247391013 scopus 로고    scopus 로고
    • Novel symmetrical substituted benzaldehyde alditol derivatives and compositions and articles containing same
    • WO: 02/077086 A2, 2002-10-03
    • John D A, Darin L D, Shawn R S et al. Novel Symmetrical Substituted Benzaldehyde Alditol Derivatives and Compositions and Articles Containing Same [P]. WO: 02/077086 A2, 2002-10-03.
    • (2002)
    • John, D.A.1    Darin, L.D.2    Shawn, R.S.3
  • 12
    • 34247369253 scopus 로고
    • Bis (3, 4-dialkylbenzylidene) sorbitol acetals and compositions containing same
    • US: 5049605, 1991-09-17
    • John W R. Bis (3, 4-dialkylbenzylidene) Sorbitol Acetals and Compositions Containing Same [P]. US: 5049605, 1991-09-17.
    • (1991)
    • John, W.R.1
  • 13
    • 34247379395 scopus 로고    scopus 로고
    • Asymmetric substituted benzaldehyde alditol derivatives and compositions and articles containing same
    • US: 6495620 B1, 2002-12-17
    • Jeffrey R J, Nathan A M. Asymmetric Substituted Benzaldehyde Alditol Derivatives and Compositions and Articles Containing Same [P]. US: 6495620 B1, 2002-12-17.
    • (2002)
    • Jeffrey, R.J.1    Nathan, A.M.2
  • 14
    • 34247371765 scopus 로고    scopus 로고
    • Novel fluorinated and alkylated alditol derivatives and compositions and polyolefin articles containing same
    • US: 2002/0062034 Al, 2002-03-23
    • John D A, Nathan A M. Novel Fluorinated and Alkylated Alditol Derivatives and Compositions and Polyolefin Articles Containing Same [P]. US: 2002/0062034 Al, 2002-03-23.
    • (2002)
    • John, D.A.1    Nathan, A.M.2
  • 15
    • 34247398224 scopus 로고    scopus 로고
    • Asymmetric monofluorinated benzaldehyde alditol derivatives and compositions and articles containing same
    • US: 6512030 B2, 2003-01-28
    • John D A, Darin L D, Jeffrey R J et al. Asymmetric Monofluorinated Benzaldehyde Alditol Derivatives and Compositions and Articles Containing Same [P]. US: 6512030 B2, 2003-01-28.
    • (2003)
    • John, D.A.1    Darin, L.D.2    Jeffrey, R.J.3
  • 16
    • 34247398224 scopus 로고    scopus 로고
    • Novel symmetrical halogenated and alkylated alditol derivatives and compositions and articles containing same
    • US: 2003/0008951 Al, 2003-01-09
    • John D A, Darin L D, Shawn R S et al. Novel Symmetrical Halogenated and Alkylated Alditol Derivatives and Compositions and Articles Containing Same [P]. US: 2003/0008951 Al, 2003-01-09.
    • (2003)
    • John, D.A.1    Darin, L.D.2    Shawn, R.S.3
  • 17
    • 2142653507 scopus 로고    scopus 로고
    • Novel class of saccharide-based organogelators: Glucofuranose derivatives as one of the smallest and highly efficient gelators
    • Roman L, Zbigniew P. Novel class of saccharide-based organogelators: Glucofuranose derivatives as one of the smallest and highly efficient gelators [J]. Tetrahedron, 2004, 60 (21): 4613-4616.
    • (2004) Tetrahedron , vol.60 , Issue.21 , pp. 4613-4616
    • Roman, L.1    Zbigniew, P.2
  • 18
    • 3042723808 scopus 로고    scopus 로고
    • Quasi-solid-state dye sensitized solar cells with 1, 3:2, 4-di-0-benzylidene-D-sorbitol derivatives as low molecular weight organic gelators
    • Mohmeyer N, Wang P, Schmidt H W et al. Quasi-solid-state dye sensitized solar cells with 1, 3:2, 4-di-0-benzylidene-D-sorbitol derivatives as low molecular weight organic gelators [J]. J Mater Chem, 2004, 14 (12): 1905-1909.
    • (2004) J Mater Chem , vol.14 , Issue.12 , pp. 1905-1909
    • Mohmeyer, N.1    Wang, P.2    Schmidt, H.W.3
  • 19
    • 0242708881 scopus 로고    scopus 로고
    • The molecular structure and intermolecular interactions of 1, 3:2, 4-dibenzylidene-D-sorbital
    • Wilder E A, Spontak R J, Hall C K. The molecular structure and intermolecular interactions of 1, 3:2, 4-dibenzylidene-D-sorbital [J]. Molecular Physics, 2003, 101 (19): 3017-3027.
    • (2003) Molecular Physics , vol.101 , Issue.19 , pp. 3017-3027
    • Wilder, E.A.1    Spontak, R.J.2    Hall, C.K.3
  • 20
    • 0038024095 scopus 로고    scopus 로고
    • Self-assembly and morphology of gel networks in 1, 3:2, 4-bis-O-(p-methylbenzylidene)-D-sorbitol/n-dibutylphthalate
    • Kobayashi T, Takenaka K, Saijo K et al. Self-assembly and morphology of gel networks in 1, 3:2, 4-bis-O-(p-methylbenzylidene)-D-sorbitol/n-dibutylphthalate [J]. Journal of Colloid and Interface Science, 2003, 262 (2): 456-465.
    • (2003) Journal of Colloid and Interface Science , vol.262 , Issue.2 , pp. 456-465
    • Kobayashi, T.1    Takenaka, K.2    Saijo, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.