907592-19-2

Upstream product

• 622-30-0 N-benzyl hydroxylalmine 
• 175877-45-9 3-C-allyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 156343-31-6 1',2'-O-isopropylidene-3'-C-(prop-1-enyl)-α-D-allyl-1',4'-furanose 
• 907592-15-8 (3aR,4aR,7aR,7bR)-2,2-dimethyl-3a,4a,7,7b-tetrahydrocyclopenta[4,5]furo[2,3-d][1,3]dioxol-7a-ol 
• 907592-17-0 (3aR,4aR,7aR,7bR)-7a-allyloxy-2,2-dimethylhexahydrocyclopenta[4,5]furo[2,3-d][1,3]dioxole 
• 907592-14-7 (3aR,5R,6R,6aR)-6-allyl-2,2-dimethyl-5-vinyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 907592-16-9 (3aR,4aR,7aR,7bR)-2,2-dimethylhexahydrocyclopenta[4,5]furo[2,3-d][1,3]dioxol-7a-ol 

Relevant academic research and scientific papers

Sequential ring-closing metathesis and nitrone cycloaddition on glucose-derived substrates: A divergent approach to analogues of spiroannulated carbanucleosides and conformationally locked nucleosides

The carbohydrate-derived substrate 3-C-allyl-1,2:5,6-di-O-isopropylidene- α-D-allofuranose was judiciously manipulated for preparing suitable synthons, which could be converted to a variety of isoxazolidino-spirocycles and -tricycles through the applicati

Synthetic studies toward highly functionalized 5β-lanosterol derivatives: A versatile approach utilizing anionic cycloaddition

Stereoselective synthesis of the potentially biologically valuable 5β-lanosteroidal-type backbone was achieved via anionic cycloaddition. Synthesis of the two new bicyclic Nazarov intermediates 14 and 40 and their cycloaddition with chiral cyclohexenone 2