1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
摘要:
Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.
1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
摘要:
Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.
1,5-Anhydro-D-fructose substituted with a hydrophobic group for use as anti-oxidant and/or emulsifier
申请人:——
公开号:US20020102342A1
公开(公告)日:2002-08-01
The present invention provides a derivatised anhydrofructose comprising a hydrophobic group linked (directly or indirectly) to a C of an anhydrofructose moiety.
本发明提供了一种衍生化的无水果糖,其包含一个疏水基团与无水果糖基团上的碳(直接或间接)连接。
1,5-ANHYDRO-D-FRUCTOSE SUBSTITUTED WITH A HYDROPHOBIC GROUP FOR USE AS ANTI-OXIDANT AND/OR EMULSIFIER
申请人:DANISCO A/S
公开号:EP1163248B1
公开(公告)日:2004-09-22
[EN] 1,5-ANHYDRO-D-FRUCTOSE SUBSTITUTED WITH A HYDROPHOBIC GROUP FOR USE AS ANTI-OXIDANT AND/OR EMULSIFIER<br/>[FR] 1,5-ANHYDRO-D-FRUCTOSE SUBSTITUEE PAR UN GROUPE HYDROPHOBE, SERVANT D'ANTI-OXYDANT ET/OU D'EMULSIFIANT
申请人:DANISCO
公开号:WO2000056745A1
公开(公告)日:2000-09-28
There is provided a derivatised anhydrofructose comprising a hydrophobic group linked (directly or indirectly) to a C of an anhydrofructose moiety.
1,5-Anhydro-d-fructose: regioselective acylation with fatty acids
作者:Søren M Andersen、Inge Lundt、Jan Marcussen、Shukun Yu
DOI:10.1016/s0008-6215(99)00163-9
日期:1999.8
Regioselective acylation of 1,5-anhydro-D-fructose was performed with dodecanoic acid to give 1,5-anhydro-6-O-dodecanoyl-D-fructose, chemically in 50% yield and enzymatically in quantitative yield. Quantitative conversions were also obtained using hexadecanoic and octadecanoic acids as acyl donors. (C) 1999 Elsevier Science Ltd. All rights reserved.