268566-41-2

Upstream product

• 186581-53-3 diazomethane 
• 268566-40-1 striatenic acid 
• 201230-82-2 carbon monoxide 
• 897049-93-3 (5R,6S)-5,6-Dimethyl-6-(2-oxo-ethyl)-cyclohex-1-enecarboxylic acid methyl ester 
• 268205-83-0 3-((6S,7R)-6,7-Dimethyl-1,4-dioxa-spiro[4.5]dec-6-yl)-propionic acid 
• 268205-82-9 3-((6S,7R)-6,7-Dimethyl-1,4-dioxa-spiro[4.5]dec-6-yl)-propionic acid methyl ester 
• 268205-84-1 4-((6S,7R)-6,7-Dimethyl-1,4-dioxa-spiro[4.5]dec-6-yl)-butan-2-one 
• 268205-88-5 (2S,3R)-2,3-Dimethyl-2-((E)-3-methyl-penta-2,4-dienyl)-cyclohexanone 
• 234077-99-7 3-((1S,2R)-1,2-Dimethyl-6-oxo-cyclohexyl)-propionic acid methyl ester 
• 897049-92-2 (5R,6R)-6-((E)-2-Methoxy-vinyl)-5,6-dimethyl-cyclohex-1-enecarboxylic acid methyl ester 
• 897049-91-1 (5R,6S)-6-Formyl-5,6-dimethyl-cyclohex-1-enecarboxylic acid methyl ester 
• 897049-94-4 (5R,6S)-5,6-Dimethyl-6-((E)-3-methyl-4-oxo-but-2-enyl)-cyclohex-1-enecarboxylic acid methyl ester 
• 2065-66-9 methyl-triphenylphosphonium iodide 

Downstream Products

• 268566-40-1 striatenic acid 

Relevant academic research and scientific papers

Improved enantioselective synthesis of natural striatenic acid and its methyl ester

This letter describes the improved and efficient enantioselective synthesis of natural striatenic acid, isolated from Cheilolejeunea serpentina, and its methyl ester starting from a readily available enantiopure building block.

Isolation and structure of striatenic acid from liverwort Cheilolejeunea serpentina and the absolute configuration by synthesis

Striatenic acid has been isolated from the liverwort Cheilolejeunea serpentina collected in Malaysia and its structure was determined on the basis of extensive 2D NMR techniques. The absolute configuration was established by synthesis of the optically act