338733-40-7Relevant articles and documents
Synthesis of a maradolipid without using protecting groups
Csuk, René,Schulthei?, Andrea,Sommerwerk, Sven,Kluge, Ralph
, p. 2274 - 2276 (2013)
A convenient route has been developed to synthesize 6-O-mono- and 6,6′-di-O-acyl symmetrical and unsymmetrical (un)-symmetrically trehalose derivatives from trehalose using a combination of enzymic and nonenzymic reactions. Thus, a typical maradolipid was accessed in two-steps.