Phosphine-catalyzed dearomative (3 + 2) annulation of 2-nitrobenzofurans and nitrobenzothiophenes with allenoates

Literature Information

Publication Date 2019-05-07
DOI 10.1039/C9OB00775J
Impact Factor 3.876
Authors

Jian-Qiang Zhao, Lei Yang, Yong You, Zhen-Hua Wang, Ke-Xin Xie, Xiao-Mei Zhang, Xiao-Ying Xu, Wei-Cheng Yuan


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Abstract

An efficient Ph2PMe-catalyzed dearomative (3 + 2) annulation of 2-nitrobenzofurans, 2-nitrobenzothiophenes, and 3-nitrobenzothiophenes with allenoates has been developed. With the developed protocol, a series of structurally important cyclopenta[b]benzofurans and cyclopenta[b]benzothiophenes were obtained in good to excellent yields (up to 98%) under mild conditions. In addition, preparative-scale experiments and transformations were conducted to exemplify the synthetic utility. The asymmetric version of this dearomative (3 + 2) annulation reaction was tentatively investigated by using chiral phosphine catalysts.

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Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
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