Synlett 2013; 24(5): 615-618
DOI: 10.1055/s-0032-1318310
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© Georg Thieme Verlag Stuttgart · New York

Total Synthesis of (±)-Spirobenzofuran

Hang Su
a   Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610 064, P. R. of China   Fax: +86(28)85413712   Email: chembliu@scu.edu.cn
,
Ting Zhou
a   Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610 064, P. R. of China   Fax: +86(28)85413712   Email: chembliu@scu.edu.cn
,
Bo Liu*
a   Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610 064, P. R. of China   Fax: +86(28)85413712   Email: chembliu@scu.edu.cn
b   Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, 345 Lingling Road, Shanghai 200 032, P. R. of China
› Author Affiliations
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Publication History

Received: 12 January 2013

Accepted after revision: 04 February 2013

Publication Date:
20 February 2013 (online)


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Abstract

Spirobenzofuran, embracing a cyclopentane-spirofused benzofuran carbon framework, was efficiently assembled via semipinacol rearrangement with Me3Al from 2,5-dimethoxy-4-methylacetophenone.

Supporting Information