863782-55-2

Upstream product

• 863782-54-1 2-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-oxirane-2-carbaldehyde 
• 90965-06-3 dimethyl 1-(1-diazo-2-oxopropyl)phosphonate 
• 186772-43-0 1-bromo-3-(tert-butyl)-5-iodobenzene 
• 89343-06-6 tris-iso-propylsilyl acetylene 
• 863782-51-8 1-tert-butyl-3-[1-(tert-butyl-dimethyl-silanyloxymethyl)-vinyl]-5-[(triisopropylsilanyl)-ethynyl]-benzene 
• 863782-53-0 (2-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-oxiranyl)-methanol 
• 863782-52-9 2-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-prop-2-en-1-ol 
• 863782-50-7 1-bromo-3-tert-butyl-5-[2-[tris(isopropyl)silyl]ethynyl]benzene 

Downstream Products

• 863782-59-6 acetic acid 1,3-bis-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-1-methyl-prop-2-ynyl ester 
• 863782-58-5 2,4-bis-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-but-3-yn-2-ol 
• 863782-56-3 2-{3-tert-butyl-5-[(triisopropylsilanyl)-ethynyl]-phenyl}-but-3-yn-2-ol 

Relevant academic research and scientific papers

Acetylenic allenophanes: An asymmetric synthesis of a bis(alleno)- bis(butadiynyl)-metacyclophane

(Chemical Equation Presented) A cyclophane with allene and acetylene bridges has been prepared as a single enantiomer. This acetylenic allenophane (see structure) was synthesized by a series of palladium- and copper-mediated coupling reactions. The allene