129006-08-2

Upstream product

• 128990-19-2 (4S)-2,2-Dimethyl-4-<(Z)-3-O-(O-methyl-L-mandeloyloxy)-2-phenylthio-2-propenoyl>-1,3-dioxolane 
• 109-92-2 ethyl vinyl ether 
• 92973-40-5 methyl (2R,3S)-3,4-O-isopropylidene-2,3,4-trihydroxybutanoate 
• 160706-48-9 1,2-O-Isopropylidene-3-O-(tetrahydropyran-2-yl)-L-threitol 
• 55137-68-3 (S)-(+)-O-methylmandeloyl chloride 
• 26164-26-1 (S)-2-methoxy-2-phenylacetic acid 
• 128990-12-5 1-Deoxy-3,4-O-isopropylidene-1-phenylthio-L-erythrulose 
• 128990-11-4 4-Deoxy-1,2-O-isopropylidene-3-phenylthio-L-threitol 
• 128990-09-0 1,2-O-Isopropylidene-4-O-methanesulfonyl-3-O-(tetrahydropyran-2-yl)-L-threitol 
• 128990-10-3 4-Deoxy-1,2-O-isopropylidene-4-phenylthio-3-O-(tetrahydropyran-2-yl)-L-threitol 
• 128990-16-9 (4S)-4-<(Z)-3-Dimethylamino-2-phenylthio-2-propenoyl>-2,2-dimethyl-1,3-dioxolane 
• 123487-66-1 Methyl 3,4-O-isopropylidene-2-O-(tetrahydropyran-2-yl)-L-threonate 
• 128990-17-0 (4S)-4-<(Z)-3-Hydroxy-2-phenylthio-2-propenoyl>-2,2-dimethyl-1,3-dioxolane 

Relevant academic research and scientific papers

Synthesis of 2-deoxy-L- and -D-galacto-heptose via inverse type hetero-Diels-Alder reaction

Inverse type hetero-Diels- Alder reaction based diastereoselective synthesis of higher sugars is performed with chiral carbon substituents in the 2-position of the 1-oxa-13-diene required as heterodiene. This is demonstrated for the synthesis of partially