120418-28-2

Upstream product

• 115463-62-2 Methyl (2R^*,3R^*,1'S^*)-(+/-)-3-hydroxy-2-(2'-methylenecyclohexan-1'-yl)butyrate 
• 120418-27-1 (2R^*,3S^*,1'R^*)-(+/-)-2-(2'-Methylenecyclohexan-1'-yl)-1,3-butanediol 
• 77-76-9 2,2-dimethoxy-propane 
• 115463-62-2 Methyl (2R^*,3S^*,1'S^*)-(+/-)-3-hydroxy-2-(2'-methylenecyclohexan-1'-yl)butyrate 
• 120418-27-1 (2R^*,3S^*,1'S^*)-(+/-)-2-(2'-Methylenecyclohexan-1'-yl)-1,3-butanediol 
• 115463-62-2 Methyl (2R^*,3S^*,1'R^*)-(+/-)-3-hydroxy-2-(2'-methylenecyclohexan-1'-yl)butyrate 
• 120418-27-1 (2R^*,3R^*,1'S^*)-(+/-)-2-(2'-Methylenecyclohexan-1'-yl)-1,3-butanediol 

Relevant academic research and scientific papers

Nucleophile-Selective Iodocyclizations: Butyrolactone versus Tetrahydrofuran Formation

Nucleophile selectivity in the electrophilic cyclization of substrates like 3 has been investigated in the context of efficient chemo- and stereoselective functionalization of 3-hydroxy-2-(2-methylenecyclohexan-1-yl)butyric acids (cf., 6-9) via iodocycliz