110815-03-7

Upstream product

• 82507-48-0 (S)-(+)-2,4-dimethylpent-4-enal 
• 82507-47-9 (S)-(-)-2,4-dimethylpent-4-en-1-ol 
• 80719-70-6 (4R,5S)-3-<(2S)-1-oxo-2,4-dimethylpent-4-enyl>-4-methyl-5-phenyloxazolidin-2-one 
• 15082-42-5 lithium benzyloxide 
• 82507-49-1 (4S,5S)-3-<(2R,3S,4S)-1-oxo-2,4,6-trimethyl-3-hydroxyhept-6-enyl>-4-methyl-5-phenyloxazolidin-2-one 
• 110902-47-1 <4-(1S,3R)-2R,4S,5S>-2-(1-naphthyl)-4-(1,3-dimethyl-4-hydroxybutyl)-5-methyl-1,3-dioxane 
• 110814-99-8 (4S)-3-<(2S,3R,4R,6S,7S,8S)-2,4,6,8-tetramethyl-3-<(trimethylsilyl)oxy>-7,9-((R)-naphthylmethylenedioxy)-1-nonanyl>-4-(1-methylethyl)-2-oxazolidinone 
• 110814-98-7 (4S)-3-<(2S,3R,4R,6S,7S,8S)-2,4,6,8-tetramethyl-3-hydroxy-7,9-((R)-naphthylmethylenedioxy)-1-oxononanyl>-4-(1-methylethyl)-2-oxazolidinone 
• 110814-97-6 <4-(1S,3R)-2R,4S,5S>-2-(1-naphthyl)-4-(1,3-dimethyl-4-oxobutyl)-5-methyl-1,3-dioxane 
• 110814-95-4 <4-(1S)-2R,4S,5S>-2-(1-naphthyl)-4-(1,3-dimethylbut-4-enyl)-5-methyl-1,3-dioxane 
• 110814-94-3 (2S,3S,4S)-2,4,6-trimethyl-1,3-dihydroxyhept-7-ene 
• 110838-51-2 benzyl (2S,3R,6S,7S,8S)-2,4,6,8-tetramethyl-3-<(trimethylsilyl)oxy>-7,9-((R)-naphthylmethylenedioxy)-1-nonanoate 
• 110815-00-4 benzyl (2S,3R,4R,6S,7S,8S)-2,4,6,8-tetramethyl-3,7,9-trihydroxy-1-nonanoate 

Downstream Products

• 110815-04-8 benzyl (2S)-2-<(2R,3R,5S,6S)-2-hydroxy-3,5-dimethyl-6-((1S)-1-methyl-2-oxoethyl)tetrahydropyran-2-yl>propanoate 

Relevant academic research and scientific papers

STUDIES DIRECTED TOWARD THE SYNTHESIS OF LYSOCELLIN CLASS POLYETHER ANTIBIOTICS. THE ASYMMETRIC SYNTHESIS OF THE C1-C9 FERENSIMYCIN SYNTHON

The asymmetric synthesis of the C1-C9 ferensimycin synthon 3 is described.The absolute stereochemical relationships in this target structure were established through chiral enolate methodology.