Synthesis of Highly Substituted Benzofuran-containing Natural Products via Rh-catalyzed Carbonylative Benzannulation-Reference-Cited by-同舟云学术

Synthesis of Highly Substituted Benzofuran-containing Natural Products via Rh-catalyzed Carbonylative Benzannulation

Published:2016-12-15 Issue:4 Volume:359 Page:693-697
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Liu Ji-tian¹²,Simmons Christopher J.¹³,Xie Haibo¹,Yang Fan¹,Zhao Xian-liang¹⁴,Tang Yu²⁵,Tang Weiping¹³

Affiliation:

1. School of Pharmacy; University of Wisconsin-Madison; Madison, WI 53705 USA

2. School of Pharmaceutical Science and Technology; Tianjin University; Tianjin 300072 P. R. China

3. Department of Chemistry; University of Wisconsin-Madison; Madison, WI 53706 USA

4. School of Biological and Chemical Engineering; Zhejiang University of Science and Technology; Hangzhou 310023 P. R. China

5. Key Laboratory of Marine Drugs; Chinese Ministry of Education; School of Medicine and Pharmacy; Ocean University of China; Qingdao 266003 P. R. China.

Publisher

Wiley

Subject

General Chemistry

Reference34 articles.

1. New oligostilbenes having a benzofuran from Vitis vinifera ‘Kyohou’

2. Five New Stilbene Dimers from the Lianas of Gnetum hainanense

3. HIV-Inhibitory and Cytotoxic Oligostilbenes from the Leaves of Hopea malibato

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