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. Author manuscript; available in PMC: 2018 Nov 24.
Published in final edited form as: Tetrahedron. 2017 Dec 21;74(25):3129–3136. doi: 10.1016/j.tet.2017.12.040

Table 2.

C-S Bond-formation: Azaarene scope.a

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a

Isolated yields of single regioisomers (unless stated otherwise) with yields of phosphonium salts in parentheses. Typical reaction conditions for C-S bond formation: 1a (0.5 mmol), thiol (0.55 mmol), NaH (0.55 mmol) and THF (2.0 mL).