1325729-80-3Relevant academic research and scientific papers
Stereoselective Strecker and carbamate annulation methodology for the synthesis of 1-amino-1,2,5-trideoxy-2,5-imino-L-iditol
Win-Mason, Anna L.,Dangerfield, Emma M.,Tyler, Peter C.,Stocker, Bridget L.,Timmer, Mattie S. M.
, p. 4008 - 4014 (2011/09/15)
An efficient and highly stereoselective synthesis of L-ido-aminoiminosugar 3 has been described. Key in the synthesis is the application of a diastereoselective Strecker reaction and the extension of our carbamate annulation methodology to protected and functionalized alkenylamines. In addition, the identification of the primary iodide as a key intermediate during the carbamate annulation reaction provides insight into the mechanism of this reaction. Copyright
Stereoselective total synthesis of aminoiminohexitols via carbamate annulation
Win-Mason, Anna L.,Jongkees, Seino A. K.,Withers, Stephen G.,Tyler, Peter C.,Timmer, Mattie S. M.,Stocker, Bridget L.
scheme or table, p. 9611 - 9621 (2012/01/03)
New methodology for the preparation of a variety of aminoiminohextitols is described. Key in the synthesis is the application of a diastereoselective Strecker reaction and the extension of our carbamate annulation methodology to protected and functionaliz
