343947-50-2

Upstream product

• 32359-01-6 hexenylmagnesium bromide 
• 103-71-9 phenyl isocyanate 
• 1483-67-6 hept-2-ynoic acid 
• 62-53-3 aniline 
• 693-02-7 hex-1-yne 

Downstream Products

• 1379964-12-1 C₁₉H₃₁NOSi 
• 1379963-38-8 C₁₉H₃₁NOSi 
• 18937-78-5 methyl 2-heptynoate 
• 1383440-77-4 C₂₀H₃₇NO₃Si₃ 
• 1383440-80-9 C₂₂H₂₅NO₃ 
• 1383440-87-6 C₂₇H₃₇NO₃Si 
• 1383440-74-1 C₂₂H₂₉NO₂Si 
• 343955-71-5 N-methyl-N-phenylhept-2-ynamide 
• 915231-65-1 N-(2-methyl-2-propenyl)-N-phenyl-2-heptynamide 

Relevant academic research and scientific papers

Catalytic oxidation/C-H functionalization of N-arylpropiolamides by means of gold carbenoids: Concise route to 3-acyloxindoles

An efficient catalytic C-H functionalization by means of gold carbenoids for the one-step synthesis of 3-acyloxindole derivatives has been developed. The reaction proceeds efficiently with extremely good substrate scope and significant opportunities for s

Platinum-catalyzed hydrosilylations of internal alkynes: Harnessing substituent effects to achieve high regioselectivity

Rule of thumb: The high yielding title reaction is described with a focus on understanding the factors that govern the regioselectivity of the process (see scheme). Electronic, steric, and functional group properties all influence the selectivity, an understanding of which allows the selective formation of trisubstituted vinylsilanes, which are synthetically useful compounds for accessing stereodefined alkenes. Copyright

Rhodium-catalyzed multicomponent-coupling reactions involving a carborhodation-cross-coupling sequence

(Chemical Equation Presented) A rhodium-catalyzed multicomponent-coupling reaction has been developed that involves a cross-coupling with organohalides as part of the reaction sequence. Through several experiments toward mechanistic investigations, it has