137423-20-2

Upstream product

• 137423-19-9 1L-(1,2,3/4)-4-Azido-1-O-(4-methoxybenzyl)-2,3-bis-O-(methoxymethyl)-5-cyclohexene-1,2,3-triol 
• 137423-14-4 Methyl 2-azido-2,6-dideoxy-6-bromo-3,4-bis-O-(methoxymethyl)-α-D-altropyranoside 
• 137423-15-5 Methyl 2-azido-2,6-dideoxy-3,4-bis-O-(methoxymethyl)-α-D-arabino-5-enopyranoside 
• 137423-17-7 2L-(2,3/4)-4-Azido-2,3-bis-O-(methoxymethyl)-2,3-dihydroxy-5-cyclohexen-1-one 
• 137423-18-8 2L-(1,2,3/4)-4-Azido-2,3-bis-O-(methoxymethyl)-5-cyclohexene-1,2,3-triol 
• 53437-75-5 methyl 2-amino-6-bromo-2,6-dideoxy-α-D-altropyranoside 

Downstream Products

• 148614-05-5 6-Bromo-benzo[1,3]dioxole-5-carboxylic acid ((1R,4R,5R,6S)-4-hydroxy-5,6-bis-methoxymethoxy-cyclohex-2-enyl)-amide 
• 137423-21-3 1L-(1,2,3/4)-4-<(6-Bromopiperonyloyl)amino>-1-O-(4-methoxybenzyl)-2,3-bis-O-(methoxymethyl)-5-cyclohexene-1,2,3-triol 
• 137423-26-8 (2S,3R,4S,4aR)-2,3,4-Triacetoxy-5-(4-methoxybenzyl)-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 
• 137423-22-4 1L-(1,2,3/4)-4-<(6-Bromopiperonyloyl)(4-methoxybenzyl)amino>-1-O-(4-methoxybenzyl)-2,3-bis-O-(methoxymethyl)-5-cyclohexene-1,2,3-triol 
• 137423-25-7 (2S,3R,4S,4aR)-2-(Benzoyloxy)-5-(4-methoxybenzyl)-3,4-bis<(methoxymethyl)oxy>-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 
• 137423-23-5 (2R,3R,4S,4aR)-5-(4-Methoxybenzyl)-2-<(4-methoxybenzyl)oxy>-3,4-bis<(methoxymethyl)oxy>-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 
• 137492-13-8 (2S,3R,4S,4aR)-2-Hydroxy-5-(4-methoxybenzyl)-3,4-bis<(methoxymethyl)oxy>-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 
• 137423-24-6 (2R,3R,4S,4aR)-2-Hydroxy-5-(4-methoxybenzyl)-3,4-bis<(methoxymethyl)oxy>-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 
• 149880-96-6 (2R,3R,4S,4aR)-2,3,4-Triacetoxy-5-(4-methoxybenzyl)-3,4,4a,5-tetrahydro<1,3>dioxolo<4,5-j>phenanthridin-6(2H)-one 

Relevant academic research and scientific papers

Total Synthesis of (+)-Lycoricidine and Its 2-Epimer from D-Glucose

Stereoselective total synthesis of antimitotic alkaloid (+)-lycoricidine (1) and its 2-epimer (30) was accomplished starting from D-glucose.The key steps in this synthesis are (i) a catalytic version of the Ferrier rearrangement for the preparation of the

Stereoselective Total Synthesis of (+)-Lycoricidine

The stereoselective total synthesis of the title compound starting from D-glucose is described.The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reactio