182282-13-9

Upstream product

• 182281-99-8 (R)-1-((2S,3S)-3-Benzyloxymethyl-3-ethyl-oxiranyl)-ethanol 
• 182282-16-2 (S)-3-Ethyl-3-(3-methoxymethoxy-propyl)-dihydro-furan-2-one 
• 182281-98-7 (E)-(R)-4-Benzyloxymethyl-hex-3-en-2-ol 
• 182281-94-3 (S,E)-2-((2,2-dimethyl-1,3-dioxolan-4-yl)methylene)butan-1-ol 
• 182282-00-4 (R)-1-((2S,3S)-3-Ethyl-3-hydroxymethyl-oxiranyl)-ethanol 
• 182282-12-8 (S)-2-Ethyl-2-(2-hydroxy-ethyl)-5-methoxymethoxy-pentanoic acid benzyl ester 
• 197848-04-7 (E)-3-(5-ethyl-2,2,4-trimethyl-1,3-dioxa-5(R)-cyclohexyl)-2-propen-1-ol 
• 197848-03-6 (E)-(R)-4-Ethyl-4-hydroxymethyl-hex-2-ene-1,5-diol 
• 182282-09-3 1-((S)-4-Ethyl-6-methoxymethoxy-4-trityloxymethyl-hexyloxymethyl)-4-methoxy-benzene 
• 182282-07-1 1-((S)-4-Ethyl-4-trityloxymethyl-hex-5-enyloxymethyl)-4-methoxy-benzene 
• 182282-08-2 (S)-3-Ethyl-6-(4-methoxy-benzyloxy)-3-trityloxymethyl-hexan-1-ol 
• 182281-97-6 Toluene-4-sulfonic acid (E)-(S)-4-benzyloxymethyl-2-hydroxy-hex-3-enyl ester 
• 182282-11-7 (S)-2-Ethyl-5-(4-methoxy-benzyloxy)-2-(2-methoxymethoxy-ethyl)-pentanoic acid 
• 182282-10-6 (S)-2-Ethyl-5-(4-methoxy-benzyloxy)-2-(2-methoxymethoxy-ethyl)-pentan-1-ol 

Relevant academic research and scientific papers

Asymmetric synthesis of key synthetic intermediates of Aspidosperma and Hunteria type indole alkaloids

Chiral synthon (6), prepared from α,β-epoxy ketone (4) via 1,2 acyl migration reaction as a key step, was converted to lactones (7) and (8), the key intermediates for Aspidosperma and Hunteria type indole alkaloids.