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Volumn 53, Issue 9, 2010, Pages 1957-1962

Synthesis and evaluation of C-glycosides as hydrotropes and solubilizing agents

Author keywords

Barbier allylation; C glycoside amphiphiles; green chemistry; Horner Wadsworth Emmons reaction; hydrotropes

Indexed keywords

ALLYLATIONS; C-GLYCOSIDE AMPHIPHILES; GREEN CHEMISTRY; HORNER-WADSWORTH-EMMONS REACTION; HYDROTROPES;

EID: 77957912644     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-010-4055-3     Document Type: Conference Paper
Times cited : (13)

References (15)
  • 3
    • 0036303578 scopus 로고    scopus 로고
    • C-glycosides by aqueous condensation of β-dicarbonyl compounds with unprotected sugars
    • 1:CAS:528:DC%2BD38Xlt1WhtrY%3D 10.1071/CH02012
    • I. Riemann M.A. Papadopoulos M. Knorst W.D. Fessner 2002 C-glycosides by aqueous condensation of β-dicarbonyl compounds with unprotected sugars Aust J Chem 55 147 154 1:CAS:528:DC%2BD38Xlt1WhtrY%3D 10.1071/CH02012
    • (2002) Aust J Chem , vol.55 , pp. 147-154
    • Riemann, I.1    Papadopoulos, M.A.2    Knorst, M.3    Fessner, W.D.4
  • 4
    • 0034699895 scopus 로고    scopus 로고
    • A convenient, one-pot, synthesis of β-C-glycosidic ketones in aqueous media
    • Rodrigues F, Canac Y, Lubineau A. A convenient, one-pot, synthesis of β-C-glycosidic ketones in aqueous media. Chem Commun, 2000: 2049-2050
    • (2000) Chem Commun , pp. 2049-2050
    • Rodrigues, F.1    Canac, Y.2    Lubineau, A.3
  • 6
    • 28244459984 scopus 로고    scopus 로고
    • A protecting group-free approach to C-glycosides using the Ramberg-Bäcklund reaction
    • DOI 10.1016/j.tetlet.2005.10.099, PII S0040403905023324
    • S. Jeanmart R.J.K. Taylor 2005 A protecting group-free approach to C-glycosides using Ramberg-Bäcklund reaction Tetrahedron Lett 46 9043 9048 1:CAS:528:DC%2BD2MXht1Git7rO 10.1016/j.tetlet.2005.10.099 (Pubitemid 41711873)
    • (2005) Tetrahedron Letters , vol.46 , Issue.52 , pp. 9043-9048
    • Jeanmart, S.1    Taylor, R.J.K.2
  • 8
    • 0002093756 scopus 로고
    • Witiig reactions on unprotected aldohexoses: Formation of optically active tetrahydrofurans and tetrahydropyrans
    • 1:CAS:528:DyaL1cXltFSkt7o%3D 10.1016/S0040-4039(00)80186-0
    • A.H. Davidson L.R. Hughes S.S. Qureshi B. Wright 1988 Witiig reactions on unprotected aldohexoses: Formation of optically active tetrahydrofurans and tetrahydropyrans Tetrahedron Lett 29 693 696 1:CAS:528:DyaL1cXltFSkt7o%3D 10.1016/S0040-4039(00)80186-0
    • (1988) Tetrahedron Lett , vol.29 , pp. 693-696
    • Davidson, A.H.1    Hughes, L.R.2    Qureshi, S.S.3    Wright, B.4
  • 9
    • 0000499542 scopus 로고
    • C-Glycosides through the Wittig-cyclization procedure: Observations on the influence of the nature of the substrate
    • 1:CAS:528:DyaL2MXhtlagtb4%3D 10.1016/S0040-4039(01)91415-7
    • F. Nicotra F. Ronchetti G. Russo L. Toma 1984 C-Glycosides through the Wittig-cyclization procedure: Observations on the influence of the nature of the substrate Tetrahedron Lett 25 5697 5700 1:CAS:528:DyaL2MXhtlagtb4%3D 10.1016/S0040-4039(01)91415-7
    • (1984) Tetrahedron Lett , vol.25 , pp. 5697-5700
    • Nicotra, F.1    Ronchetti, F.2    Russo, G.3    Toma, L.4
  • 10
    • 77149137074 scopus 로고    scopus 로고
    • Horner-Wadsworth-Emmons reaction of unprotected sugars in water or in the absence of any solvent: One-step access to C-glycoside amphiphiles
    • Ranoux A, Lemiègre L, Benoit M, Guégan JP, Benvegnu T. Horner-Wadsworth-Emmons reaction of unprotected sugars in water or in the absence of any solvent: One-step access to C-glycoside amphiphiles. Eur J Org Chem, 2010: 1314-1323
    • (2010) Eur J Org Chem , pp. 1314-1323
    • Ranoux, A.1
  • 11
    • 34548113536 scopus 로고    scopus 로고
    • Hydrotropic solutions
    • DOI 10.1016/j.cocis.2007.06.004, PII S135902940700060X
    • T.K. Hodgdon E.W. Kaler 2007 Hydrotropic solutions Cur Opin Colloid Interf Sci 12 121 128 1:CAS:528:DC%2BD2sXpsV2qtL8%3D 10.1016/j.cocis.2007.06.004 (Pubitemid 47302357)
    • (2007) Current Opinion in Colloid and Interface Science , vol.12 , Issue.3 , pp. 121-128
    • Hodgdon, T.K.1    Kaler, E.W.2
  • 12
    • 23144458069 scopus 로고    scopus 로고
    • Unified concept of solubilization in water by hydrotropes and cosolvents
    • DOI 10.1021/la050554l
    • P. Bauduin A. Renoncourt A. Kopf D. Touraud W. Kunz 2005 Unified concept of solubilization in water by hydrotropes and cosolvents Langmuir 21 6769 6775 1:CAS:528:DC%2BD2MXltVyms74%3D 10.1021/la050554l (Pubitemid 41084464)
    • (2005) Langmuir , vol.21 , Issue.15 , pp. 6769-6775
    • Bauduin, P.1    Renoncourt, A.2    Kopf, A.3    Touraud, D.4    Kunz, W.5
  • 13
    • 0026045466 scopus 로고
    • Organometallic reactions in aqueous media with indium
    • 1:CAS:528:DyaK38Xkt1Grur0%3D 10.1016/0040-4039(91)85028-4
    • C.J. Li T.H. Chan 1991 Organometallic reactions in aqueous media with indium Tetrahedron Lett 32 7017 7020 1:CAS:528:DyaK38Xkt1Grur0%3D 10.1016/0040-4039(91)85028-4
    • (1991) Tetrahedron Lett , vol.32 , pp. 7017-7020
    • Li, C.J.1    Chan, T.H.2
  • 14
    • 27944484827 scopus 로고    scopus 로고
    • Rapid and solvent-free synthesis of homoallyl or homopropargyl alcohols mediated by zinc powder
    • Wang JX, Jia X, Meng T, Xin L. Rapid and solvent-free synthesis of homoallyl or homopropargyl alcohols mediated by zinc powder. Synthesis 2005: 2838-2844
    • (2005) Synthesis , pp. 2838-2844
    • Wang, J.X.1    Jia, X.2    Meng, T.3    Xin, L.4
  • 15
    • 0037433608 scopus 로고    scopus 로고
    • Development of a highly α-regioselective metal-mediated allylation reaction in aqueous media: New mechanistic proposal for the origin of α-homoallylic alcohols
    • DOI 10.1021/ja029276s
    • K.T. Tan S.S. Chng H.S. Cheng T.P. Loh 2003 Development of a highly α-regioselective metal-mediated allylation reaction in aqueous media: New mechanistic proposal for the origin of α-homoallylic alcohols J Am Chem Soc 125 2958 2963 1:CAS:528:DC%2BD3sXhtFeksLc%3D 10.1021/ja029276s (Pubitemid 36512521)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.10 , pp. 2958-2963
    • Tan, K.-T.1    Chng, S.-S.2    Cheng, H.-S.3    Loh, T.-P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.