1422178-75-3

Upstream product

• 1422178-74-2 C₃₃H₄₂O₇ 
• 100-39-0 benzyl bromide 
• 1422178-70-8 (2R,3R,4S,5S,6S)-4,6,7-tris(benzyloxy)heptane-1,2,3,5-tetraol 
• 96-22-0 pentan-3-one 
• 1422178-71-9 C₃₁H₃₈O₇ 

Downstream Products

• 1422178-76-4 (2R,3R,4S,5S,6S)-3,4,5,6,7-pentakis(benzyloxy)heptane-1,2-diol 

Relevant academic research and scientific papers

Synthesis of C(27)-C(38) fragment of aflastatin A

Efforts at finding out a strategy for the synthesis of the densely hydroxylated C(27)-C(48) fragment of aflastatin A have been described. The initial studies dealing with alkyne-epoxide coupling using a linear polyol epoxide resulted in a debenzylative cycloetherification leading to a C-arabinoside derivative. This problem has been addressed by applying an epoxide pendant on a furanosyl unit. With the model alkyne, the epoxide-alkyne coupling proceeded smoothly. Subsequently, following a sequence of [Pd]-mediated alkynone cycloisomerization/stereoselective hydroboration-oxidation, the synthesis of the central C(27)-C(38) fragment has been executed. When employed, the original C(33)-C(48) alkyne, the coupling and the cycloisomerizations are facile. However, the resulting glycals are unstable, thus warranting a revision in our approach.