138457-70-2

Upstream product

• 133886-01-8 2-azido-2-deoxy-6-O-benzyl-3,4-O-isopropylidene-β-D-psico-furanose 
• 133886-05-2 1-β-Azido-1-dehydro-1-α-carboxy-1-deoxy-2,3-O-isopropylidene-5-O-benzyl-D-ribofuranose 
• 133886-04-1 2-β-Azido-2-deoxy-6-O-benzyl-1-didehydro-3,4-O-isopropylidene-D-psicofuranose 
• 133886-06-3 1-β-Azido-1-dehydro-1-α-carbamoyl-1-deoxy-2,3-O-isopropylidene-5-O-benzyl-D-ribofuranose 

Downstream Products

• 179559-93-4 (3aR,6R,6aR)-6-Benzyloxymethyl-4-[3-(4-methoxy-benzyl)-ureido]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid amide 
• 130607-23-7 <2R,3S,4R,5R>-2-Benzyloxymethyl-3,4-dihydroxy-1-oxa-6,8-diazaspiro<4.4>nonane-7,9-dione 
• 130607-24-8 <2R,3S,4R,5S>-2-Benzyloxymethyl-3,4-dihydroxy-1-oxa-6,8-diazaspiro<4.4>nonane-7,9-dione 
• 130607-26-0 [5S-(5α,7α,8β,9β)]-1,3-diaza-8,9-dihydroxy-7-(hydroxymethyl)-6-oxaspiro[4.4]nonane-2,4-dione 
• 129744-46-3 <2R,3R,4R,5S>-6-N-Acetyl-2-benzyloxymethyl-3,4-isopropylidene-1-oxa-6,8-diazaspiro<4.4>nonane-7,9-dione 
• 133908-92-6 <2R,3R,4R,5S>-6-N-Acetyl-2-benzyloxymethyl-3,4-dihydroxy-1-oxa-6,8-diazaspiro<4.4>nonane-7,9-dione 
• 138379-98-3 (3aR,6R,6aR)-6-Benzyloxymethyl-2,2-dimethyl-4-ureido-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid amide 
• 138379-99-4 (3R,4S,5R)-5-Benzyloxymethyl-3,4-dihydroxy-2-ureido-tetrahydro-furan-2-carboxylic acid amide 
• 129744-45-2 [5S-(5α,7α,8β,9β)]-7-(benzyloxymethyl)-8,9-isopropylidenedioxy-6-oxa-1,3-diazaspiro[4.4]nonane-2,4-dione 
• 133908-91-5 [5R-(5α,7β,8α,9α)]-7-(benzyloxymethyl)-1,3-diaza-8,9-isopropylidenedioxy-6-oxaspiro[4.4]nonane-2,4-dione 

Relevant academic research and scientific papers

Synthetic studies on (+)-hydantocidin (3): A new synthetic method for construction of the spiro-hydantoin ring at the anomeric position of D-ribofuranose

A facile synthetic route for the large-scale preparation of a herbicidal natural product, (+)-hydantocidin is described. The protected D-psicose 6, prepared in five steps from D-fructose, was stereospecifically converted to azido-amide 14 by N-glycosidation (TMSN3/TMSOTf), oxidation and animation. Hydantoin ring-construction on 14 was achieved by aza-Wittig reaction (PBu3/CO2/CH3CN) to give 16 without epimerization at the anomeric center. After acetylation, stepwise deprotection of 24 afforded (+)-hydantocidin 1 in 16% overall yield from D-fructose.