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Two Approaches to Diverting the Course of a Free-Radical Cyclization: Application of Cyclopropylcarbinyl Radical Fragmentations and Allenes as Radical Acceptors

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NIAID Data Ecosystem2026-03-06 收录
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Free radical cyclization of 4 and 7 gave the expected cyclization-reduction products (5 and 8) along with considerable amounts of products derived from a cyclization−atom transfer−secondary cyclization process (6 and 9). Two approaches to avoiding these unexpected products were explored. Use of a cyclopropylcarbinyl fragmentation avoided the secondary cyclization reaction (25 or 43 → 26 or 44), whereas use of an allene as a radical acceptor avoided the atom-transfer reaction altogether (49 → 52).

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2016-02-25
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