474958-64-0

Upstream product

• 150-76-5 4-methoxy-phenol 
• 474958-62-8 (1S,2S)-2-p-methoxyphenyloxy-1-phenyl-but-3-en-1-ol 
• 474958-61-7 B-γ-p-methoxyphenoxyallyldiisopinocampheylborane 
• 13391-35-0 allyl (4-methoxyphenyl) ether 

Downstream Products

• 474958-68-4 [(1R,2S,3R)-2,3-bis-(p-methoxyphenyloxy)-3-phenyl-1-(prop-2-enyl)-propyl]-prop-2-enoate 
• 474958-66-2 (2R,3R)-2,3-bis-(p-methoxyphenyloxy)-3-phenylpropanal 

Relevant academic research and scientific papers

Cross-metathesis/iridium(I)-catalyzed allylic etherification strategy: (Iterative) catalytic asymmetric synthesis of syn- and anti-1,2-diols

Protection optional: The title reaction strategy is used to prepare 1,2-diols with complete control of their absolute and relative stereochemistry. The method tolerates free and Me-/Bn-/TBS-protected alcohol functionalities, and its diastereoselectivity i

Stereoselective syntheses of (+)-goniodiol, (-)-8-epigoniodiol, and (+)-9-deoxygoniopypyrone via alkoxyallylboration and ring-closing metathesis

A convenient synthesis of (+)-goniodiol, (-)-8-epigoniodiol, and (+)-9-deoxygoniopypyrone has been developed via asymmetric alkoxyallylboration and ring-closing metathesis pathways.