796128-14-8

Upstream product

• 100-39-0 benzyl bromide 
• 149859-05-2 1-[2',2'-dimethyl-(4'R)-1',3'-dioxolan-4'-yl]-(1S)-3-butyn-1-ol 
• 383135-46-4 2,2'-dimethyl-1-(4'(R)-1',3'-dioxacyclopentyl)-but-3-yn-1(S/R)-ol 

Downstream Products

• 1160926-68-0 3,4-O-isopropylidene-2-O-benzyl-1-deoxy-1-C-[(1-(2-nitrophenyl)-1H-1,2,3-triazol-4-yl)]-D-erythritol 
• 58871-14-0 (3-benzyloxy-3,4-dihydro-2H-pyran-2-yl)-methanol 
• 117399-55-0 1,5-anhydro-4,6-di-O-benzyl-D-erythro-hex-1-enitol 

Relevant academic research and scientific papers

N -Alkynyl Pyrrole Based Total Synthesis of Shensongine A

A copper-catalyzed N-alkynylation of pyrrole and a gold-catalyzed spiroketalization were key steps in the total synthesis of the pyrrole spiroketal alkaloid shensongine A. The preparation of this alkaloid is concise and amenable to the rapid synthesis of

A flexible approach toward trans-fused polycyclic tetrahydropyrans. A synthesis of prymnesin and yessotoxin units

(Chemical Equation Presented) Ru-catalyzed cycloisomerization and oxidative cyclization of bis-homopropargylic alcohols provide a rapid iterative approach to structural units of the ladder toxins.