340013-57-2

Upstream product

• 3396-99-4 methyl α-D-galactopyranoside 
• 181480-80-8 6-O-tert-butyldimethylsilanyl-1-O-methyl-α-D-galactopyranoside 
• 305834-18-8 (2S,3R,4S,5R)-3,4,5-tris(benzyloxy)-2-(iodomethyl)-6-methoxytetrahydro-2H-pyran 
• 4356-80-3 methyl 2,3,4-tri-O-benzyl-α-D-galactopyranoside 
• 35904-60-0 methyl 6-deoxy-6-iodo-α-D-galactopyranoside 
• 340013-40-3 C₂₉H₃₂O₅ 

Downstream Products

• 340013-58-3 1-Methoxy-4-((1S,4S,5R,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyloxymethyl)-benzene 
• 223524-30-9 (1S,4S,5R,6S)-4,5,6-Tris-benzyloxy-cyclohex-2-enol 

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

A new convergent route to aldohexoses from a common chiral building block.

[reaction in text] A diastereocontrolled route to the eight aldohexoses has been developed starting from a common cyclohexanoid chiral building block.