623151-41-7

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 88158-68-3 4-(tert-butyldiphenylsilyloxy)-1-butyne 
• 107-19-7 propargyl alcohol 
• 246514-55-6 (1E)-4-(tert-butyldiphenylsilanyloxy)-1-iodobut-1-ene 

Downstream Products

• 623151-52-0 2-[(1E,6Z,8E)-(4R,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-11-(tert-butyl-diphenyl-silanyloxy)-4-methyl-undeca-1,6,8-trienyl]-[1,3]dioxane 
• 623151-47-3 (2E,7Z,9E)-(5R,6R)-6-(tert-butyldimethylsilanyloxy)-12-(tert-butyldiphenylsilanyloxy)-5-methyldodeca-2,7,9-trienoic acid N-methoxy-N-methylamide 
• 623151-53-1 2-{1-(tert-butyl-dimethyl-silanyloxy)-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-methyl-2,3,3a,4,5,7a-hexahydro-1H-inden-4-yl}-[1,3]dioxane 
• 623151-44-0 (7E)-(3R,4R)-4-(tert-butyldimethylsilanyloxy)-10-(tert-butyldiphenylsilanyloxy)-3-methyldec-7-en-5-yn-1-ol 
• 623151-48-4 (2E,7Z,9E)-(5R,6R)-6-(tert-butyldimethylsilanyloxy)-12-(tert-butyldiphenylsilanyloxy)-5-methyldodeca-2,7,9-trienal 
• 623151-45-1 (5Z,7E)-(3R,4R)-4-(tert-butyldimethylsilanyloxy)-10-(tert-butyldiphenylsilanyloxy)-3-methyldeca-5,7-dien-1-ol 
• 623151-43-9 (3E)-(7R,8R)-7-(tert-butyldimethylsilanyloxy)-1-(tert-butyldiphenylsilanyloxy)-8-methyldeca-3,9-dien-5-yne 
• 623151-46-2 (5Z,7E)-(3R,4R)-4-(tert-butyldimethylsilanyloxy)-10-(tert-butyldiphenylsilanyloxy)-3-methyldeca-5,7-dienal 
• 623151-54-2 1-(tert-butyl-dimethyl-silanyloxy)-5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2-methyl-2,3,3a,4,5,7a-hexahydro-1H-indene-4-carbaldehyde 
• 623151-42-8 (4E)-7-(tert-butyldiphenylsilanyloxy)hept-4-en-2-ynal 

Relevant academic research and scientific papers

Probing the Lewis Acid-Catalyzed Intramolecular Diels-Alder Cyclizations of Allylic Alkoxy-Substituted (Z)-1,3-Dienes

(Matrix presented) The Lewis acid-promoted Diels-Alder reaction of (E,Z,E)-trienal 1 provides not only the expected cis-fused cycloadduct 16 but also the transfused products 17 and 18. Trans-fused cycloadducts 17 and 18 are also products of the Lewis acid