661490-76-2

Upstream product

• 661490-67-1 [(S)-1-(2-Benzyloxy-ethyl)-allyloxy]-acetic acid 
• 117661-29-7 (3S)-3-hydroxy-5-benzyloxy-1-pentene 
• 117661-29-7 5-(benzyloxy)pent-1-en-3-ol 
• 105104-40-3 Okahara's reagent 
• 70905-45-2 1,3-dichloro-2-(methoxymethoxy)propane 
• 108270-19-5 3-iodo-2-(methoxymethyloxy)-1-propene 
• 661490-69-3 (S)-3-{2-[(S)-1-(2-Benzyloxy-ethyl)-allyloxy]-acetyl}-4-isopropyl-oxazolidin-2-one 

Downstream Products

• 661490-80-8 (S)-3-[(2R,6S)-6-(2-Benzyloxy-ethyl)-4-methoxymethoxy-3,6-dihydro-2H-pyran-2-carbonyl]-4-isopropyl-oxazolidin-2-one 

Relevant academic research and scientific papers

A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.