85687-32-7Relevant academic research and scientific papers
A New Stereoselective Route to Branched-Chain Nitro and Amino Sugars: Synthesis of Both Enantiomers of Decilonitrose and Avidinosamine
Greven, Ralph,Juetten, Peter,Scharf, Hans-Dieter
, p. 3742 - 3747 (2007/10/02)
Short, efficient, and highly diastereoselective syntheses of the title carbohydrates (15, 21, and 22), components of new anthracycline antibiotics, on a gram scale from readily available keto sugar precursors 6 and 17 are described.The syntheses feature t
Branched-chain Sugars. Part 18. Syntheses of D-Rubranitrose (2,3,6-Trideoxy-3-C-methyl-4-O-methyl-3-nitro-D-xylo-hexopyranose) and a Derivative of D-Kijanose (2,3,4,6-Tetradeoxy-4-methoxycarbonylamino-3-methyl-3-nitro-α-D-xylo-hexopyranose)
Brimacombe, John S.,Rahman, Khandker M. M.
, p. 1073 - 1080 (2007/10/02)
D-Rubranitrose (2,3,6-trideoxy-3-C-methyl-4-O-methyl-3-nitro-D-xylo-hexopyranose) (22), a constituent of the antibiotic rubradirin, has been synthesized from methyl 3,31-anhydro-4,6-O-benzylidene-2-deoxy-3-C-(hydroxymethyl)-α-D-arabino-hexopyr
SYNTHESIS AND ANTITUMOR ACTIVITY OF 3'-C-METHYL-DAUNORUBICIN
Thang, Ton That,Imbach, Jean Louis,Fizames, Christian,Lavelle, Francois,Ponsinet, Gerard,et al.
, p. 241 - 248 (2007/10/02)
Reaction of 1,5-anhydro-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-trifluoroacetamido-L-lyxo-hex-1-enitol with daunomycinone in the presence of anhydrous toluene-p-sulfonic acid in benzene, followed by removal of the N- and O-protecting groups under mild con
