552314-05-3

Upstream product

• 100-39-0 benzyl bromide 
• 552314-09-7 (3S)-2,2-dimethyl-3-(tetrahydropyran-2-yloxy)pent-4-en-1-ol 
• 147331-80-4 (3R)-dihydro-4,4-dimethyl-3-(2-tetrahydropyranyloxy)-2(3H)-furanone 
• 599-04-2 (R)-Pantolacton 
• 110-87-2 3,4-dihydro-2H-pyran 
• 220343-35-1 (2RS,3R)-1-oxa-2-hydroxy-3-[tetrahydropyran-2(RS)-yloxy]-4,4-dimethylcyclopentane 

Downstream Products

• 220774-56-1 (4S)-4-((3RS)-2-Methyl-3-hydroxy-5-phenyl-pent-2-yl)-2,2-dimethyl-[1,3]dioxane 
• 849061-55-8 3-((S)-2,2-Dimethyl-[1,3]dioxan-4-yl)-3-methyl-1-phenyl-butan-2-ol 
• 224968-23-4 (4S)-4-(2-benzyloxy-1,1-dimethylethyl)-2,2-dimethyl[1,3]dioxane 
• 152426-81-8 (3S)-1-benzyloxy-2,2-dimethylpentane-3,5-diol 
• 552314-06-4 (3S)-5-benzyloxy-4,4-dimethyl-3-(tetrahydropyran-2-yloxy)pentan-1-ol 

Relevant academic research and scientific papers

Efficient chiral pool synthesis of the C1-C6 fragment of epothilones

An efficient chiral pool synthesis of the C1-C6 fragment of epothilones starting from readily available (-)-pantolactone is described.

C1-C6-epothilone fragments and process for the production of C1-C6-fragments of epothilones and derivatives thereof

This invention describes C1-C6-epothilone fragments and an efficient process for the production of C1-C6-fragments of epothilones and derivatives thereof.