The synthesis of quaternary carbon centers through cyclialkylations

DOI: 10.1016/S0040-4039(98)01931-5

Source and publish data:

Tetrahedron Letters p. 8381 - 8384 (1998)

Update date:2022-08-04

Topics:

Authors:

Majetich, George

Fang, Jing

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Article abstract of DOI:10.1016/S0040-4039(98)01931-5

Treatment of conjugated dienone 1 with a strong Lewis acid at -78 °C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system.

Full text of DOI:10.1016/S0040-4039(98)01931-5

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