117016-13-4

Upstream product

• 21204-32-0 ε-iso-rhodomycinone 
• 132814-67-6 1-O-tert-butyldimethylsilyl 4-O-p-nitrobenzoyl-2,3,6-trideoxy-3-trifluoroacetamido-β-L-lyxo-hexopyranoside 
• 77398-05-1 (2S,3S,4S)-2-methyl-3-(4-nitrobenzoyloxy)-4-trifluoracetamido-3,4-dihydro-2H-pyran 

Downstream Products

• 127903-57-5 7-O-<2,3,6-Trideoxy-3-<6(S)-hydroxymethyl-2(S)-methoxymorpholin-4-yl>-α-L-lyxo-hexopyranosyl>-ε-isorhodomycinone 
• 127903-57-5 7-O-<2,3,6-Trideoxy-3-<6(S)-hydroxymethyl-2(R)-methoxymorpholin-4-yl>-α-L-lyxo-hexopyranosyl>-ε-isorhodomycinone 
• 127903-63-3 7-O-<2,3,6-Trideoxy-3-(morpholin-4-yl)-α-L-lyxo-hexopyranosyl>-ε-isorhodomycinone 
• 117016-15-6 7-O-(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)-ε-isorhodomycinone 

Relevant academic research and scientific papers

Semisynthetic ε-(iso)rhodomycins: a new glycosylation variant and modification reactions

Synthesis of 7-O-(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)-ε-(iso)rhodomycinones 16 and 17, and their 3'-morpholino derivatives are described.Glycosylation (trimethylsilyl triflate, 10:1 dichloromethane-acetone, -35 deg C) of 1-O-tert-butyldimethyls

Semisynthetic ε-isorhodomycins: their synthesis using glycals and their structure-activity relationship

Syntheses and structure-activity relationships of 7-O-(3-amino-2,3,6-trideoxy-α-L-lyxo- (18), -L-arabino- (20) and -L-ribo-hexopyranosyl)-ε-isorhodomycins (25) and their 3'-dimethylamino derivatives 22, 23 and 26 are described.Condensation (trimethylsilyl