An approach to (±)-Lingzhiol
2016; American Chemical Society; Volume: 18; Issue: 8 Linguagem: Inglês
10.1021/acs.orglett.6b00542
ISSN1523-7060
AutoresXiaoyu Li, Xiaoyu Liu, Xiaozhen Jiao, Hongguang Yang, Yangyang Yao, Ping Xie,
Tópico(s)Fungal Biology and Applications
Resumo(±)-Lingzhiol has been synthesized from commercially available 5,8-dimethoxytetralone in seven steps with an overall yield of 10.3% via an unprecedented acid-catalyzed semipinacol-type rearrangement. In addition, a novel strategy for the construction of the tetracyclic 5/5/6/6 core structure of lingzhiol has been developed via a tandem rearrangement/reduction/lactonization reaction.
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