1370531-93-3

Upstream product

• 1353687-51-0 (4S,5S)-4-((benzyloxy)methyl)-5-ethynyl-2,2-dimethyl-1,3-dioxolane 
• 1370531-92-2 C₁₅H₁₇BrO₃ 
• 156647-91-5 (R)-(-)-8-Nonin-2-ol 
• 78469-77-9 (4S,5S)-4-benzyloxymethyl-5-hydroxymethyl-2,2-dimethyl-1,3-dioxolane 
• 81028-12-8 (4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-5-carboxaldehyde 
• 693-02-7 hex-1-yne 
• 156715-27-4 (R)-(-)-4-Nonin-2-ol 

Relevant academic research and scientific papers

Alkyne-assisted approach to the formal synthesis of antibiotic macrolide (-)-A26771B

A stereoselective formal synthesis of a 16-membered antibiotic macrolide (-)-A26771B is described starting from (R)-propylene oxide and (+)-diethyl tartrate. Key steps involved in this alkyne-assisted convergent approach are alkyne zipper reaction, Cadiot