117708-33-5

Upstream product

• 117653-55-1 (4R,5S)-2,3-Dimethyl-5-phenylsulfanylmethyl-4-(tetrahydro-pyran-2-yloxymethyl)-cyclopent-2-enone 
• 102368-38-7 3,4-dimethyl-4-hydroxy-5-<(methoxymethyl)oxy>-1-<(2-tetrahydropyranyl)oxy>-2,5,6-heptatriene 
• 162340-83-2 2,3-Dimethyl-5-methylene-4-<<(tetrahydropyran-2-yl)oxy>methyl>-2-cyclopenten-1-one 

Downstream Products

• 117653-57-3 tert-Butyl-[(1S,4R,5S)-2,3-dimethyl-5-phenylsulfanylmethyl-4-(tetrahydro-pyran-2-yloxymethyl)-cyclopent-2-enyloxy]-dimethyl-silane 
• 117653-58-4 [(1R,2S,3S,4S,5S)-3-Benzenesulfonylmethyl-1,5-dimethyl-4-(tetrahydro-pyran-2-yloxymethyl)-6-oxa-bicyclo[3.1.0]hex-2-yloxy]-tert-butyl-dimethyl-silane 
• 117653-58-4 [(1R,2R,3R,4R,5S)-3-Benzenesulfonylmethyl-1,5-dimethyl-4-(tetrahydro-pyran-2-yloxymethyl)-6-oxa-bicyclo[3.1.0]hex-2-yloxy]-tert-butyl-dimethyl-silane 
• 117653-59-5 (1S,2R,3R,4R,5R)-3-Benzenesulfonylmethyl-1,5-dimethyl-4-(tetrahydro-pyran-2-yloxymethyl)-6-oxa-bicyclo[3.1.0]hexan-2-ol 
• 117653-59-5 (1S,2S,3S,4S,5R)-3-Benzenesulfonylmethyl-1,5-dimethyl-4-(tetrahydro-pyran-2-yloxymethyl)-6-oxa-bicyclo[3.1.0]hexan-2-ol 

Relevant academic research and scientific papers

A Concise Synthesis of d,l-Methylenomycin A and d,l-epi-Methylenomycin A

A cationic cyclopentaannelation reaction that was developed in our laboratories has been applied to the synthesis of d,l-methylenomycin A, a fungal metabolite that has been isolated from a strain of Streptomyces violaceoruber.The efficiency of the key rea