1268630-63-2

Upstream product

• 130748-67-3 (2S)-N-(4-methylbenzene)-1-sulfonoamido-4-methylpentan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 7533-40-6 (S)-2-amino-4-methylpentan-1-ol 
• 1268631-05-5 C₂₉H₅₅NO₄SSi₂ 
• 316363-73-2 (S)-O-(tert-butyldimethylsilyl)-N-(4-methylbenzenesulfonyl)-leucinol 

Downstream Products

• 1268630-72-3 C₁₇H₂₅NO₃S 

Relevant academic research and scientific papers

Gold-catalyzed direct activation of allylic alcohols in the stereoselective synthesis of functionalized 2-vinyl-morpholines

Alcohol versus alcohol: A highly stereocontrolled synthesis of substituted morpholines is realized by means of gold-catalyzed dehydrative allylic cyclization of diols (see scheme for one example; segphos = 5,5′-bis[di(3, 5-di-tert-butyl-4-methyoxyphenyl)phosphine]-4,4′-bi-1,3-benzodioxole). The present methodology represents one of the few examples of enantioselective gold-catalyzed transformations involving unactivated alkenes. Copyright