CAS: 211567-22-5; (2R,3S,4R,5R,6R)-5-Acetamido-2-(Acetoxymethyl)-6-(Dodecyloxy)Tetrahydro-2H-Pyran-3,4-Diyl Diacetate

相似化合物

147025-06-7 173725-22-9 115431-24-8

上下游产品

1-dodecyl alcohol Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 2-acetamido-3,4,6-tri-O-acetyl-D-glucopyranosyl acetatedodecyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside 1-dodecyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 5-phospha-cyclopenta[a]naphthalen-2-yl)-amineBis-(2-chloro-ethyl)-((3aR,4R,5aR,8R,9aR,9bS)-4-dodecyloxy-2-oxo-8-phenyl-°Ctahydro-1,5,7,9-tetraoxa-3-aza-2λ5-phospha-cyclopenta[a]naphthalen-2-yl)-amine Methanesulfonic acid (2R,4aR,6R,7R,8R,8aR)-7-acetylamino-6-dodecyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester

📜十二烷醇,(3Ar)-2-甲基-5Alpha-(乙酰氧基甲基)-6Beta,7Alpha-二乙酰氧基-3Aalpha,6,7,7Aalpha-四氢-5H-吡喃并[3,2-D]恶唑置于对甲苯磺酸体系中,用 1,2-二氯乙烷 用作溶剂,以82%的收率获得十二烷基-2,3,4,6-四-氧-乙酰基-β-D-吡喃氨基葡萄糖苷
参考文献:Synthesis And Protective Anti-Infective Action Of Anomeric Lipophilic Glycosides Of N-Acetylmuramyl-L-Alanyl-D-Isoglutamine
标题:Synthesis And Protective Anti-Infective Action Of Anomeric Lipophilic Glycosides Of N-Acetylmuramyl-L-Alanyl-D-Isoglutamine
摘要:Anomeric Pairs Of Alpha-And Beta-Dodecyl,Alpha-And Beta-(1-Pentylhexyl),And Alpha-And Beta-Cyclododecyl Glycosides Of N-Acetylmuramyl-L-Alanyl-D-Isoglutamine (Mdp) Were Synthesized. The Starting Beta-D-Glucosaminides Were Obtained By The Oxazoline Method,And The Corresponding Alpha-Isomers,By The Mercuric Iodide-Catalyzed Glycosylation Of Alcohols With Alpha-Glucosaminyl Chloride Peracetate In Nitromethane At-90 Degrees C. No Reliable Differences Between The Stimulation Of Mouse Resistance To The Infection With Staphylococcus Aureus (Doses Of 2,20,And 200 Mu G/mouse) And Escherichia Coli (Doses Of 0.05,1,And 20 Mu G/mouse) With The Mdp Alpha-And Beta-Glycosides Were Found.
Doi:10.1134/s1068162006040091