113974-07-5Relevant academic research and scientific papers
Stereoselective total syntheses of the naturally occurring enantiomers of N-acetylneuraminic acid and 3-deoxy-D-manno-2-octulosonic acid. A new and stereospecific approach to sialo and 3-deoxy-D-manno-2-octulosonic acid conjugates
Danishefsky,DeNinno,Chen
, p. 3929 - 3940 (2007/10/02)
The total syntheses of the title compounds have been achieved. A critical element of these syntheses was the concept of using a furan ring as a surrogate for a carboxylic acid. The furyl diene 22 reacted with the R and S enantiomers of 2-(phenylseleno)pro
The Total Synthesis of (+/-)-N-Acetylneuraminic Acid (NANA): A Remarkable Hydroxylation of a (Z)-Enoate
Danishefsky, Samuel J.,DeNinno, Michael P.
, p. 2615 - 2617 (2007/10/02)
A total synthesis of the title compound was achieved.A key feature of the synthesis involved a stereospecific hydroxylation of a (Z)-carbomethoxyvinyl pyranoside.
