288402-96-0

Upstream product

• 148407-40-3 (2R,3R)-3-undecyloxirane-2-methanol 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 139623-13-5 (R)-1,3-dihydroxytetradecane 

Downstream Products

• 637741-19-6 (1R,2S,3R)-1-[(4-methoxybenzyloxy)methyl]-2,3-bis(4-methoxybenzyloxy)-4-(tert-butyldimethylsiloxy)butyl (2E,4R,5S,6E,8E,11R)-2,4,6,8-tetramethyl-5-(triethylsiloxy)-11-(4-methoxybenzyloxy)-2,6,8-docosatrienoate 
• 637742-07-5 (2E,6E,8E)-(4R,5S,11R)-5-Hydroxy-11-(4-methoxy-benzyloxy)-2,4,6,8-tetramethyl-docosa-2,6,8-trienoic acid (1R,2S,3R)-4-hydroxy-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-butyl ester 
• 637742-31-5 (2E,6E,8E)-(4R,11R)-11-(4-Methoxy-benzyloxy)-2,4,6,8-tetramethyl-5-oxo-docosa-2,6,8-trienoic acid (1R,2R,3S)-3-carboxy-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-propyl ester 
• 637742-06-4 (2E,6E,8E)-(4R,5S,11R)-11-(4-Methoxy-benzyloxy)-2,4,6,8-tetramethyl-5-triethylsilanyloxy-docosa-2,6,8-trienoic acid 
• 637742-04-2 (2E,6E,8E)-(4R,5S,11R)-11-(4-Methoxy-benzyloxy)-2,4,6,8-tetramethyl-5-triethylsilanyloxy-docosa-2,6,8-trienoic acid ethyl ester 
• 637742-05-3 (2E,6E,8E)-(4R,5S,11R)-11-(4-Methoxy-benzyloxy)-2,4,6,8-tetramethyl-5-triethylsilanyloxy-docosa-2,6,8-trien-1-ol 
• 637742-01-9 (4E,6E)-(2S,3S,9R)-9-(4-Methoxy-benzyloxy)-2,4,6-trimethyl-3-triethylsilanyloxy-icosa-4,6-dienethioic acid S-ethyl ester 
• 637742-03-1 (4E,6E)-(2S,3S,9R)-9-(4-Methoxy-benzyloxy)-2,4,6-trimethyl-3-triethylsilanyloxy-icosa-4,6-dienal 
• 637741-18-5 S-ethyl (2S,3S,4E,6E,9R)-2,4,6-trimethyl-3-hydroxy-9-(4-methoxybenzyloxy)-4,6-icosadienethioate 
• 637741-17-4 (2E,4E,7R)-2,4-dimethyl-7-(4-methoxybenzyloxy)-2,4-octadecadien-1-ol 
• 637742-00-8 (2E,4E)-(R)-7-(4-Methoxy-benzyloxy)-2,4-dimethyl-octadeca-2,4-dienal 
• 637741-98-1 (E)-(R)-5-(4-Methoxy-benzyloxy)-2-methyl-hexadec-2-en-1-ol 
• 637742-30-4 (E)-(R)-5-(4-Methoxy-benzyloxy)-2-methyl-hexadec-2-enal 
• 637741-97-0 (R)-3-(4-methoxybenzyloxy)tetradecanal 

Relevant academic research and scientific papers

Chemistry and biology of khafrefungin. Large-scale synthesis, design, and structure-activity relationship of khafrefungin, an antifungal agent

Large-scale synthesis, design, and structure-activity relationships of khafrefungin are reported. Khafrefungin is an antifungal agent that inhibits inositol phosphorylceramide (IPC) synthase, a enzyme involved in fungal sphingolipid biosynthesis. Unlike o

Synthesis of lipid A type pyran carboxylic acids with ether chains and their biological activities

Synthesis of lipid A type pyran carboxylic acids having ether chains at both the C-3′ and C-4 positions and their bioactivities toward human U937 cells are described.