259877-35-5

Upstream product

• 1200119-23-8 C₂₁H₂₆O₄ 
• 762-72-1 allyl-trimethyl-silane 
• 95990-81-1 Dithiocarbonic acid O-((3R,4S,5R)-4-benzyloxy-5-benzyloxymethyl-2-methoxy-tetrahydro-furan-3-yl) ester S-methyl ester 
• 102339-30-0 (3R,4R,5R)-4-(benzyloxy)-5-(benzyloxymethyl)-2-methoxytetrahydrofuran-3-ol 
• 219661-90-2 (2R,3R)-3-(benzyloxy)-2-(benzyloxymethyl)-5-methoxytetrahydrofuran 

Relevant academic research and scientific papers

The stereoselective total synthesis of PF1163A

A stereoselective total synthesis of 13-membered macrocycle PF1163A, an antifungal agent, has been accomplished for the first time starting from d-xylose. This approach involves a diastereoselective allylation of lactal ether,3a reductive ring

Highly diastereoselective allylation of lactols and their ethers using molecular iodine

Lactols and their ethers undergo smooth allylation with allyltrimethylsilane in the presence of 5 mol % iodine in dichloromethane at -78 °C to afford C-allylfuranosides in good yields and with high diastereoselectivity. The use of iodine makes this method