64929-15-3

Upstream product

• 71327-31-6 dehydroisoerivanin 
• 59444-49-4 C₁₅H₁₈O₅ 
• 185432-27-3 (3S,3aS,5aS,9bS)-8-Hydroxy-3,5a,9-trimethyl-3a,4,5,5a,8,9b-hexahydro-3H-naphtho[1,2-b]furan-2-one 
• 117152-29-1 C₁₅H₂₀O₅ 
• 481-06-1 santonin 
• 59444-49-4 C₁₅H₁₈O₅ 
• 423769-23-7 santonin 

Relevant academic research and scientific papers

SESQUITERPENE LACTONES OF ARTEMISIA MEXICANA VAR. ANGUSTIFOLIA

Seven eudesmanolides were isolated and characterized from Artemisia mexicana var. angustifolia.These included arglanin, artemexifolin, ludalbin, santamarine and three new compunds named 8α-acetoxyarmexifolin, α-epoxyludalbin and armefolin.The structure of armexifolin is revised.Key Word Index - Artemisia mexicana var. angustifolia; Compositae; sesquiterpene lactones; 8α-acetoxyarmexifolin; α-epoxyludalbin; armefolin.

Short-step synthesis of some santanolides, dehydroisoerivanin, isoerivanin, ludovicin C, and 1α,3α-dihydroxyarbusculin B by the use of the organoselenium reduction method of epoxy ketones

Short-step synthesis of four santanolides, dehydroisoerivanin (1), isoerivanin (2), ludovicin C (3), and 1α,3α-dihydroxyarbusculin B (4) is described in which the organoselenium reduction of a cross diepoxy ketone was involved as a key step.

Synthesis of Dehydroisoerivanin, Isoerivanin, Ludovicin C, and 1α,3α-Dihydroxyarbusculin B Utilizing the Organoselenium-mediated Reduction of Epoxy Ketone

Short step synthesis of dehydroisoerivanin, isoerivanin, ludovicin C, and 1α,3α-dihydroxyarbusculin B have been achieved by employing the organoselenium-mediated reduction of α,β-epoxy ketone as the key step.