124991-87-3

Upstream product

• 10229-11-5 4-phenyl-but-3-yn-1-ol 
• 85375-43-5 4-methyl-N-(4-phenylbut-3-yn-1-yl)benzenesulfonamide 

Downstream Products

• 135056-60-9 3-[1-Phenyl-meth-(E)-ylidene]-octahydro-inden-4-one 
• 154414-61-6 Bis(4-phenylbut-3-ynyl) diselenide 
• 124943-55-1 3-(4-Phenyl-but-3-ynyl)-azepan-2-one 
• 166535-84-8 3-(4-phenylbut-3-ynyl)piperidin-2-one 
• 164169-57-7 dimethyl(5-phenylpent-4-ynyl)silane 
• 622-76-4 1-phenyl-1-butyne 
• 130602-12-9 8-phenyl-7-octyn-2-one 

Relevant academic research and scientific papers

Indirect electroreductive sequential radical reaction catalyzed by a Ni(II) complex. One-step preparation of functionalized (methylene)cyclopentanes

Substituted (methylene)cyclopentanes were prepared by one-step reaction at room temperature from butynyl iodides and activated olefins by sequencing of free radical addition and cyclization reactions. The reactions, which were conducted by indirect electroreduction catalyzed by a nickel(II) complex, proceeded with modest selectivity for formation of the Z(methylene)cyclopentanes.

Intramolecular N-(Acyloxy)iminium Ion-Alkyne Cycloadditions. A New Route to Bicyclic α-Amino Ketones

The intramolecular cyclocondensation of 15 cyclic N-(acyloxy)iminium cations containing tethered alkyne and alkene nucleophiles is reported (eqs 5 and 6).This route to heterotricyclic systems was specifically demonstrated with substrates in which the hete