137986-87-9

Upstream product

• 93-97-0 benzoic acid anhydride 
• 137986-88-0 methyl 12-benzyloxy-7β-hydroxypodocarpa-8,11,13-trien-19-oate 
• 137986-88-0 methyl 12-benzyloxy-7α-hydroxypodocarpa-8,11,13-trien-19-oate 
• 137986-89-1 methyl 12-benzoyloxy-7β-hydroxypodocarpa-8,11,13-trien-19-oate 
• 137987-00-9 methyl 12-benzoyloxy-7-oxopodocarpa-8,11,13-trien-19-oate 
• 137987-15-6 methyl 12-benzoyloxypodocarpa-8,11,13-trien-19-oate 
• 137986-99-3 methyl 12-benzyloxy-7-oxopodocarpa-8,11,13-trien-19-oate 
• 137986-83-5 methyl 12-benzyloxypodocarpa-6,8,11,13-tetraen-19-oate 
• 138125-87-8 12-acetoxy-7-oxopodocarpic acid methyl ester 
• 137986-91-5 methyl 7β,12-dihydroxypodocarpa-8,11,13-trien-19-oate 
• 137986-85-7 methyl 12-hydroxypodocarpa-6,8,11,13-tetraen-19-oate 
• 55025-16-6 methyl (1S,4aS,10aR)-6-(benzyloxy)-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylate 
• 31979-05-2 7-Oxo-podocarpensaeure-methylester 
• 4614-56-6 methyl podocarpate 

Relevant academic research and scientific papers

Reaction of Podocarpa-6,8,11,13-tetraenes with m-Chloroperbenzoic Acid and Dimethyldioxiran: Synthesis of Methyl 6α,7α-Epoxy-12-methoxy-podocarpa-8,11,13-trien-19-oate

The reaction of some podocarpa-6,8,11,13-tetraenes with m-chloroperbenzoic acid in either a one-phase system or a two-phase system with an aqueous buffer leads to epoxide-opened products.Successful epoxidations have been achieved in high yield by using th