138489-29-9

Upstream product

• 104115-47-1 (7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-one 
• 104115-45-9 N-<2-(2-Methyl-1,3-dioxolan-2-yl)ethyl>-2-oxocyclopentaneacetamide 
• 138489-25-5 (3aR,6aS)-6a-Hydroxy-1-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-hexahydro-cyclopenta[b]pyrrol-2-one 
• 104115-46-0 (7aR^*,10aS^*)-(+/-)-Hexahydrospiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-one 
• 138489-24-4 (+/-)-(1R^*,5S^*)-1-hydroxy-2-azabicyclo<3.3.0>octan-3-one 
• 138489-23-3 (3aS,6aR)-6a-Chloro-hexahydro-cyclopenta[b]furan-2-one 
• 62240-37-3 2-(2-methyl-1,3-dioxolane-2-yl)ethan-1-amine 
• 37865-96-6 2-(2-bromoethyl)-2-methyl-1,3-dioxolane 
• 84764-41-0 2-(2-(2-methyl-1,3-dioxolan-2-yl)ethyl)isoindoline-1,3-dione 
• 104115-44-8 (2-oxocyclopent)acetic acid 

Downstream Products

• 138489-31-3 C₃₄H₅₃NO₄SSi 

Relevant academic research and scientific papers

Daphniphyllum Alkaloids. 10. Classical Total Synthesis of Methyl Homodaphniphyllate

Details for the first total synthesis of a Daphniphyllum alkaloid are presented.The synthesis required a total of 15 steps from the known keto acid 4 and followed the course 4 -> 10 -> 11 -> 16 -> 20 -> 24 -> 25 -> 27 -> 29 -> 36 -> 46 -> 47 -> 48 -> 49 -