155155-66-1

Upstream product

• 958643-54-4 methyl 2,3-di-O-benzyl-6-deoxy-6-iodo-α-D-mannopyranoside 
• 1313193-62-2 C₂₁H₂₄O₅ 
• 155049-46-0 methyl 2,3,4-tri-O-benzyl-5-methylene-α-D-lyxopyranoside 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 206186-94-9 methyl 2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-α-D-mannopyranoside 

Downstream Products

• 1313193-65-5 (4R,5R,6S)-4,5,6-tris(benzyloxy)-2-iodocyclohex-2-en-1-one 
• 1313193-66-6 (4R,5R,6S)-4,5,6-tris(benzyloxy)-2-methylcyclohex-2-enone 
• 127545-53-3 (4R,5R,6S)-4,5,6-trihydroxy-2-methyl-2-cyclohexen-1-one 
• 6195-80-8 2,4-bis(benzyloxy)phenol 
• 144668-26-8 (2S,3R,4R,5R)-2,3,4-Tris-benzyloxy-5-methyl-cyclohexanone 

Relevant academic research and scientific papers

Chiron approach to the total synthesis of Amaryllidaceae alkaloid (+)-lycoricidine

A highly stereoselective total synthesis of Amaryllidaceae alkaloid starting from α-D-galactopyranoside has been described. The salient features of this total synthesis are Ferrier carbocyclization reaction for the synthesis of ring A and Suzuki Miyaura c

Syntheses of (-)-gabosine A, (+)-4-epi-gabosine A, (-)-gabosine E, and (+)-4-epi-gabosine e

(+)-4-epi-Gabosine A 1 and (-)-gabosine A 2 have been synthesized starting from methyl α,d-glucopyranoside and methyl α,d-mannopyranoside, respectively, by utilizing Pd(0) catalyzed Stille coupling as the key step. On the other hand, syntheses of (+)-4-ep