1377418-97-7

Upstream product

• 6485-40-1 (R)-Carvone 
• 99-48-9 (4R,6R)-carveol 
• 917987-31-6 tert-butyldimethyl(((1R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl)oxy)silane 
• 1377419-08-3 (2S,3R,5R)-3-((tert-butyldimethylsilyl)oxy)-2-(2-((1R,6S)-6-hydroxy-1-methylcyclohex-2-en-1-yl)ethyl)-5-isopropyl-2-methylcyclopentanone 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 1377418-96-6 (R)-2-(2-((1S,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-oxocyclopentyl)ethyl)-2-methylcyclohex-3-enone 
• 1377419-07-2 (1R,2R)-2-(2-((1S,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-oxocyclopentyl)ethyl)-2-methyl-3-oxocyclohexyl methanesulfonate 
• 1377418-95-5 (2R,3R)-2-(2-((1S,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-oxocyclopentyl)ethyl)-3-hydroxy-2-methylcyclohexanone 
• 1377418-94-4 2-(2-((1S,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-oxocyclopentyl)ethyl)-2-methylcyclohexane-1,3-dione 
• 1377418-93-3 2-(2-((1R,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-methylenecyclopentyl)ethyl)-2-methylcyclohexane-1,3-dione 
• 1377419-05-0 2-(2-((1R,3R,5R)-5-((tert-butyldimethylsilyl)oxy)-3-isopropyl-1-methyl-2-methylenecyclopentyl)ethyl)cyclohexane-1,3-dione 
• 1377418-91-1 tert-butyl((1R,4R)-4-isopropyl-2-methyl-3-(vinyloxymethyl)cyclopent-2-enyloxy)dimethylsilane 
• 1377418-92-2 2-((1R,3R,5R)-5-(tert-butyldimethylsilyloxy)-3-isopropyl-1-methyl-2-methylenecyclopentyl)acetaldehyde 

Downstream Products

• 1377419-09-4 (4R,5S)-4-((tert-butyldimethylsilyl)oxy)-5-(2-((1R,6S)-6-((tertbutyldimethylsilyl)oxy)-1-methylcyclohex-2-en-1-yl)ethyl)-2-isopropyl-5-methylcyclopent-1-en-1-yl trifluoromethanesulfonate 
• 1377418-98-8 (4R,5S)-4-((tert-butyldimethylsilyl)oxy)-5-(2-((1R,6S)-6-((tertbutyldimethylsilyl)oxy)-1-methyl-4-oxocyclohex-2-en-1-yl)ethyl)-2-isopropyl-5-methylcyclopent-1-en-1-yl trifluoromethanesulfonate 

Relevant academic research and scientific papers

Total synthesis of cyrneine A

Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample. Copyright