Observations on the nature of the tethering chain in the synthesis of biaryls and heterobiaryls via intramolecular free radical ipso substitution reactions
✍ Scribed by Maria Lucília E.N. da Mata; William B. Motherwell; Feroze Ujjainwalla
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 223 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A study of benzylic sulfonates and their corresponding N-methylsulphonamide derivatives as substrates in potential free radical [1,6] ipso substitution reactions reveals a preference for the alternative [1,7] addition mode. Empirical guidelines for biaryl and heterobia~l synthesis using this approach can then be made.
📜 SIMILAR VOLUMES
Hindered biaryls and heterobiaryls are even easier to prepare by intramolecular free radical [1,5] ipso substition using sulfonamide and sulfonate tethering chains, since the introduction of either electron releasing or electron withdrawing groups ortho to the sulfonyl substituted acceptor ring faci
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