1373485-72-3

Upstream product

• 204905-77-1 3,4-ethylenedioxythiophene-2-carboxaldehyde 
• 126213-50-1 3,4-(ethylenedioxy)thiophene 
• 1373485-40-5 (2,3-dihydro-5-(5,5-dimethyl-1,3-dioxan-2-yl)thieno[3,4-b][1,4]dioxin-7-yl)-N,N-dimethylmethanamine 
• 1373485-60-9 7-(3,4,5-trimethoxystyryl)-2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carbaldehyde 
• 304891-35-8 [4-(diethoxyphorylmethyl)-2,5-bis(2-ethylhexyloxy)benzyl]phosphonic acid diethyl ester 
• 1373485-51-8 5-(3,4,5-trimethoxystyryl)-2,3-dihydro-7-(5,5-dimethyl-1,3-dioxan-2-yl)thieno[3,4-b][1,4]dioxine 
• 1373485-41-6 [7-(5,5-dimethyl-[1,3]dioxan-2-yl)-2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-ylmethyl]trimethyliodineamine 
• 1286685-26-4 5-(5,5-dimethyl-[1,3]dioxin-2-yl)-2,3-dihydro-thieno[3,4-b][1,4]dioxine 

Relevant academic research and scientific papers

Sequence-independent synthesis of π-conjugated arylenevinylene oligomers using bifunctional thiophene monomers

Sequence-independent or "click" chemistry is applied for the preparation of a series of novel and structurally similar π-conjugated oligomers. The new oligomers are prepared using Wittig-Horner chemistry from bifunctional building blocks that can be inter