oxygen; anhydrous cobalt diacetate; triphenylphosphine multistep reaction: 1.) 75 deg C; other temperatures (25, 50 deg C); other catalyst (ABIN); autooxidation of olefins, reduction of the hydroperoxides formed; Product distribution;

<b>With</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '107477', constants.ctx, '0')">quinoline</a>;&nbsp;<a href="#" onclick="return RXDsubstances(event, this, '19497626', constants.ctx, '0')">Pd-BaSO₄</a>;&nbsp;<a href="#" onclick="return RXDsubstances(event, this, '3587189', constants.ctx, '0')">hydrogen</a>&nbsp;<b>in</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '969132', constants.ctx, '0')">pentane</a> <br />2.5&nbsp;h;&nbsp;<br /> &nbsp;

<b>With</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '107477', constants.ctx, '0')">quinoline</a>;&nbsp;<a href="#" onclick="return RXDsubstances(event, this, '3587189', constants.ctx, '0')">hydrogen</a>;&nbsp;<a href="#" onclick="return RXDsubstances(event, this, '11378939', constants.ctx, '0')">Lindlar's catalyst</a>&nbsp;<b>in</b>&nbsp; various solvent(s)<br />&nbsp;Yield given. Yields of byproduct given. Title compound not separated from byproducts;&nbsp;<br /> &nbsp;

<b>With</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '3587189', constants.ctx, '0')">hydrogen</a>;&nbsp;<a href="#" onclick="return RXDsubstances(event, this, '19240558', constants.ctx, '0')">Lindlar's catalyst</a>&nbsp;<b>in</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '1718733', constants.ctx, '0')">ethanol</a> <br /> <br /> &nbsp;

<b>With</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '11342956', constants.ctx, '0')">selenium</a> <br />T=100&deg;C;&nbsp;18&nbsp;h;&nbsp;<br /> &nbsp;