1187486-36-7

Upstream product

• 66221-85-0 2-bromooctyl phenyl selenide 
• 34837-55-3 Phenylselenyl bromide 
• 63831-85-6 1-phenylseleno-1-octene 
• 111-66-0 oct-1-ene 

Downstream Products

• 1187486-47-0 di-(-)-menthyl 2-hexylcyclopropane-1,1-dicarboxylate 
• 1187486-42-5 di-(-)-menthyl 2-hexylcyclopropane-1,1-dicarboxylate 
• 1235455-21-6 (2R,3R,5R)-5-hexyl-2,3-diphenyl-1,4-dioxane 
• 1235455-09-0 (2R,3R,5S)-5-hexyl-2,3-diphenyl-1,4-dioxane 
• 1268165-97-4 (2S,5R)-4-benzyl-2-hexyl-5-phenylmorpholine 
• 1268165-99-6 (2R,5R)-4-benzyl-2-hexyl-5-phenylmorpholine 

Relevant academic research and scientific papers

Synthesis of oxazino[4,3-a]indoles by domino addition-cyclization reactions of (1H-indol-2-yl)methanols and vinyl selenones in the presence of 18-crown-6

Herein we report the synthesis of biologically relevant oxazino[4,3-a]indoles by an environmentally friendly Michael addition-cyclization cascade using potassium hydroxide in dichloromethane employing variously substituted vinyl selenones and (1H-indol-2y

Synthesis of enantiopure 1,4-dioxanes, morpholines, and piperazines from the reaction of chiral 1,2-diols, amino alcohols, and diamines with vinyl selenones

The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-aminoalcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedu