535994-33-3

Upstream product

• 2234-82-4 1-propylmagnesium chloride 
• 535994-47-9 3-(dimethyl(phenyl)silyl)prop-2-yn-1-yl methanesulfonate 
• 43019-63-2 3-(phenyldimethylsilyl)prop-2-yn-1-ol 
• 128792-89-2 hex-2-yn-1-yl methyl carbonate 
• 185990-03-8 dimethylphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silane 
• 764-60-3 hex-2-yn-1-ol 

Downstream Products

• 871268-72-3 C₃₆H₆₂O₃Si₃ 
• 871268-73-4 (2S,3R,4R)-2-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-4-(dimethyl-phenyl-silanyl)-4-vinyl-heptan-3-ol 
• 871268-74-5 (2S,3S,4S)-2-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-4-(dimethyl-phenyl-silanyl)-4-vinyl-heptan-3-ol 

Relevant academic research and scientific papers

Cu-Catalyzed silylation of alkynes: A traceless 2-pyridylsulfonyl controller allows access to either regioisomer on demand

The Cu-catalyzed silylation of terminal and internal alkynes bearing a 2-pyridyl sulfonyl group (SO2Py) at the propargylic position affords a breadth of vinyl silanes in good yields and with excellent regio- and stereocontrol under mild conditi

Enantio- and diastereoselective synthesis of cyclic β-hydroxy allylsilanes via sequential aldehyde γ-silylallylboration and ring-closing metathesis reactions

(Matrix presented) Highly enantioenriched cyclic allylsilanes are prepared via stereoselective γ-silylallylboration reactions of β- or γ-unsaturated aldehydes followed by ring-closing metathesis.