263011-59-2

Upstream product

• 263011-57-0 (2S,3R)-3-((S)-2-Benzyloxy-1-methyl-ethyl)-oxirane-2-carbaldehyde 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 263011-58-1 (3S,4S)-5-Benzyloxy-3-hydroxy-4-methyl-pentanal 
• 81520-03-8 (2E,4R)-5-(benzyloxy)-4-methyl-2-penten-1-ol 
• 81520-05-0 [(2R,3R)-3-((S)-2-Benzyloxy-1-methyl-ethyl)-oxiranyl]-methanol 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 

Downstream Products

• 263011-60-5 ethyl {(4R,6S)-6-[(S)-2-(benzyloxy)-1-methylethyl]-2-phenyl-1,3-dioxan-4-yl}acetate 
• 263011-62-7 (Z)-4-[(4S,6S)-6-((S)-2-Benzyloxy-1-methyl-ethyl)-2-phenyl-[1,3]dioxan-4-yl]-but-2-enoic acid ethyl ester 
• 263011-61-6 [(4R,6S)-6-((S)-2-Benzyloxy-1-methyl-ethyl)-2-phenyl-[1,3]dioxan-4-yl]-acetaldehyde 
• 263011-63-8 (S)-6-((2S,3S)-4-Benzyloxy-2-hydroxy-3-methyl-butyl)-5,6-dihydro-pyran-2-one 
• 263011-66-1 (2S,3S)-4-Benzyloxy-1-((S)-6-methoxy-3,6-dihydro-2H-pyran-2-yl)-3-methyl-butan-2-ol 

Relevant academic research and scientific papers

The stereoselective synthesis of the C6-C18 fragment of scytophycin C employing a novel synthetic methodology

A novel synthetic approach towards the stereoselective synthesis of the C6-C18 fragment of the biologically active antitumor agent scytophycin C is described. The synthesis involves Marouka allylation, base-catalyzed intramolecular conjugate addition, Wit

An efficient and stereoselective construction of the C(9)-C(17) dihydropyran segment of swinholides A-C via a novel reductive cleavage of an epoxy aldehyde

An efficient and highly stereoselective construction of the C(9)-C(17) dihydropyran segment of swinholides A-C, which involves a novel reductive cleavage of an epoxy aldehyde by an organoselenium reagent and the intramolecular conjugate addition of an ace