476461-13-9

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 476461-12-8 2-(S)-(2,2-dibromovinyl)-6-(S)-methoxytetrahydropyran-4-(R)-ol 
• 476461-11-7 tert-butyl-[2-(S)-(2,2-dibromovinyl)-6-(S)-methoxytetrahydropyran-4-(R)-yloxy]-dimethylsilane 
• 91312-61-7 methyl 3-O-(tert-butyldimethylsilyl)-2,4-dideoxy-6-O-(triphenylmethyl)-α-D-erythro-hexapyranoside 
• 91312-68-4 methyl 3-O-(tert-butyldimethylsilyl)-2,4-dideoxy-6-oxo-α-D-erythro-hexopyranoside 
• 91312-63-9 methyl 3-O-(tert-butyldimethylsilyl)-2,4-dideoxy-6-hydroxy-α-D-erythro-hexopyranoside 

Downstream Products

• 476461-15-1 methanesulfonic acid 3-[6-(S)-methoxy-4-(R)-(4-methoxybenzyloxy)-tetrahydropyran-2-(S)-yl]-prop-2-ynyl ester 
• 476461-16-2 C₄₂H₅₀O₁₄ 
• 476461-08-2 C₅₄H₇₈O₁₄Si₂ 
• 476461-14-0 3-[6-(S)-methoxy-4-(R)-(4-methoxybenzyloxy)-tetrahydropyran-2-(S)-yl]-prop-2-yn-1-ol 

Relevant academic research and scientific papers

Highly Selective Entry to the Azadirachtin Skeleton via a Claisen Rearrangement/Radical Cyclization Sequence

(Matrix Presented) A highly diastereoselective, microwave-induced Claisen rearrangement of an appropriately substituted propargylic enol ether allows the formation of the sterically congested C8-C14 bond of azadirachtin. When combine