124356-84-9

Upstream product

• 78-85-3 2-methylpropenal 
• 101712-01-0 (S)-1-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-methylpentane-1,3-dione 
• 101712-01-0 (R)-1-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-methylpentane-1,3-dione 
• 124356-91-8 (4R)-3-[(2R,3S)-3-hydroxy-2-methyl-pentanoyl]-4-benzyl-oxazolidine-2-one 
• 101711-78-8 (3R)-3-propionyl-4-benzyloxazolidin-2-one 

Downstream Products

• 124356-87-2 [[3-(2S,3R,4S,5R)-4S]-3-(3,5-dihydroxy-2,4,6-trimethyl-1-oxohept-6-enyl)-4-(phenylmethyl)]-2-oxazolidinone 
• 124356-93-0 <3(2S,4R,5S),6S>-3-<1-oxo-2-<2,2,5-trimethyl-4-(1-methylethenyl)-1,3-dioxan-6-yl>propyl>-4-(phenylmethyl)-2-oxazolidinone 
• 124379-81-3 (4S)-4-benzyl-3-<(2S,4R,5S,6R)-5-hydroxy-6-<(4S,5R,6R)-6-isopropenyl-2,2,5-trimethyl-1,3-dioxan-4-yl>-2,4-dimethyl-3-oxoheptanoyl>-2-oxazolidinone 
• 124356-90-7 (4S)-4-benzyl-3-<(2S,4R,5S,6R)-5-methoxy-6-<(4S,5R,6R)-6-isopropenyl-2,2,5-trimethyl-1,3-dioxan-4-yl>-2,4-dimethyl-3-oxoheptanoyl>-2-oxazolidinone 
• 129618-46-8 (S)-2-{(4R,5S,6S)-6-[(1R,2S,3R,5S)-6-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-methoxy-1,3,5-trimethyl-4,6-dioxo-hexyl]-2,2,5-trimethyl-[1,3]dioxan-4-yl}-propionaldehyde 
• 129618-45-7 (2S,4R,5S,6R)-1-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-6-[(4S,5R,6S)-6-((R)-2-hydroxy-1-methyl-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-5-methoxy-2,4-dimethyl-heptane-1,3-dione 
• 129618-45-7 (2S,4R,5S,6R)-1-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-6-[(4S,5R,6S)-6-((S)-2-hydroxy-1-methyl-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-5-methoxy-2,4-dimethyl-heptane-1,3-dione 
• 129618-44-6 (S)-4-Benzyl-3-((S)-2-{(2R,3R,4S,5R,6S)-2,4-dimethoxy-3,5-dimethyl-6-[(R)-1-((4R,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-ethyl]-tetrahydro-pyran-2-yl}-propionyl)-oxazolidin-2-one 

Relevant academic research and scientific papers

Total synthesis of the polyether antibiotic lonomycin A (Emericid)

The first asymmetric synthesis of the polyether antibiotic lonomycin has been achieved. The skeleton is assembled through the synthesis and union of two subunits comprising the C1-C11 and C12-C30 portions of the

Diastereoselective anti aldol reactions of chiral ethyl ketones. Enantioselective processes for the synthesis of polypropionate natural products

The diastereoselective anti aldol reactions of the β-keto imide 3a, the related ethyl ketone 20b, and its diastereomer 22b have been studied. In these aldol reactions, the chiral ethyl ketones 3a and 20b were found to exhibit the opposite sense of asymmet