394738-18-2

Upstream product

• 394738-12-6 benzoic (2S,5S)-5-(1-benzenesulfonyl-1-nitroethyl)-2,5-dihydrofuran-2-yl ester 
• 263887-24-7 4-hydroxy-3-(4-methoxyphenylmethoxy)benzaldehyde 
• 394738-13-7 4-[(2S,5S)-5-(1-benzenesulfonyl-1-nitroethyl)-2,5-dihydrofuran-2-yloxy]-3-(4-methoxybenzyloxy)-benzaldehyde 

Downstream Products

• 419572-66-0 (E)-3-[4-[(3aR,4S,6S,6aS)-6-(1-Benzenesulfonyl-1-nitro-ethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxy]-3-(4-methoxy-benzyloxy)-phenyl]-2-methyl-acrylic acid ethyl ester 
• 419572-63-7 (E)-3-{4-[(3aR,4S,6S,6aR)-6-(1-benzenesulfonyl-1-nitroethyl)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yloxy]-3-(4-methoxybenzyloxy)-phenyl}-2-methylacrylic acid 
• 11049-00-6 C-2-epi-hygromycin A 
• 394738-19-3 (E)-3-{4-[(2S,3R,4S,5S)-5-(1-Benzenesulfonyl-1-nitro-ethyl)-3,4-dihydroxy-tetrahydro-furan-2-yloxy]-3-hydroxy-phenyl}-2-methyl-acrylic acid ethyl ester 
• 394738-20-6 (E)-3-{4-[(3aR,4S,6S,6aR)-6-(1-benzenesulfonyl-1-nitroethyl)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yloxy]-3-hydroxyphenyl}-2-methylacrylic ethyl ester 
• 394738-15-9 (E)-3-{4-[(3aR,4S,6S,6aS)-6-(1-Benzenesulfonyl-1-nitro-ethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxy]-3-hydroxy-phenyl}-2-methyl-acrylic acid 
• 394738-17-1 (E)-3-{4-[(3aR,4S,6S,6aR)-2,2-dimethyl-6-(2-methyl-[1,3]dioxolan-2-yl)-tetrahydrofuro[3,4-d][1,3]dioxol-4-yloxy]-3-hydroxyphenyl}-2-methylacrylic acid 
• 394738-16-0 (E)-3-{4-[(3aR,4S,6S,6aR)-6-acetyl-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yloxy]-3-hydroxyphenyl}-2-methylacrylic acid 
• 394738-14-8 (E)-3-{4-[(2S,3R,4S,5S)-5-(1-benzenesulfonyl-1-nitroethyl)-3,4-dihydroxy-tetrahydrofuran-2-yloxy]-3-(4-methoxybenzyloxy)-phenyl}-2-methylacrylic ethyl ester 

Relevant academic research and scientific papers

Application of the AAA reaction to the synthesis of the furanoside of C-2-epi-hygromycin A: A total synthesis of C-2-epi-hygromycin A

A strategy for stereocontrolled syntheses of furanoside type of natural products is developed for a glycosyl aryl ether. This strategy resolves the issue of low diastereoselectivity typical of normal glycosidation methods for furanosides. All the stereoch

An asymmetric synthesis of c-2-epi-hygromycin a

The power of Pd-catalyzed asymmetric allylic alkylation (AAA) reactions is clearly demonstrated by the efficient synthesis of the complex title compound 1, an analogue of hygromycin A. The modular nature of the synthetic route is ideally suited to provide