20097-40-9Relevant articles and documents
A short and efficient route from myo - To neo -inositol
Wessig, Pablo,M?llnitz, Kristian,Hübner, Sebastian
scheme or table, p. 1497 - 1500 (2010/09/05)
An efficient route from myo- to neo-inositol is described. The key steps of the sequence are oxidation of the hydroxy group at C-5 to the corresponding ketone, followed by a highly (dr = 7.8:1) stereoselective reduction. The route includes nine steps with an overall yield of 51% and is therefore superior to all hitherto reported methods for the preparation of neo-inositol. Georg Thieme Verlag Stuttgart New York.
Protecting group-directed, diastereoselective samarium diiodide-promoted carbocyclization: Application to the synthesis of cyclitols
Carpintero, Mercedes,Fernandez-Mayoralas, Alfonso,Jaramillo, Carlos
, p. 1916 - 1917 (2007/10/03)
-
The structure of adenomycin (C19-97 substance)
Ogita,Otake,Miyazaki,et al.
, p. 3203 - 3206 (2007/10/02)
-