114375-29-0Relevant academic research and scientific papers
Stereoselective reactions of alkenylpyranosides: The effect of double bond geometry on conformation
DeNinno,Danishefsky,Schulte
, p. 3925 - 3929 (2007/10/02)
For purposes of stereochemical analysis, alkenylpyranosides have been subdivided into E and Z versions of two classes differing by whether the double bond is or is not conjugated with an electron-withdrawing function (cf. ester). Ground-state solid-state
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.
