BF3 ⋅ Et2O‐Mediated Annulation of 2‐Alkynyl Biaryls with N‐(Arylthio) Succinimides: An Efficient Approach to Access 9‐Sulfenylphenanthrenes

BF3 ⋅ Et2O-Mediated Annulation of 2-Alkynyl Biaryls with N-(Arylthio) Succinimides: An Efficient Approach to Access 9-Sulfenylphenanthrenes

A simple and effective method for the synthesis of 9-sulfenylphenanthrenes was developed. The reaction proceeds through BF3 ⋅ OEt2-mediated annulation of 2-alkynyl biaryls with N-arylthio succinimides at room temperature. With this method, a series of 9-sulfenylphenanthrenes was efficiently obtained in good to excellent yields under mild and metal-free conditions.


Abstract

A simple and effective method for the synthesis of 9-sulfenylphenanthrenes was developed via BF3 ⋅ OEt2-mediated annulation of 2-alkynyl biaryls with N-arylthio succinimides at room temperature. Through this methodology, a series of 9-sulfenylphenanthrenes could be efficiently and conveniently obtained in good to excellent yields under mild and metal-free conditions.