An Efficient Synthesis of Dibenzo[b,f]oxepins by Ring-Closing Metathesis

被引：15

作者：

Bharath, Yada ^{[1
]}

Thirupathi, Barla ^{[1
]}

Ranjit, Gurram ^{[1
]}

Mohapatra, Debendra K. ^{[1
]}

机构：

[1] Indian Inst Chem Technol, CSIR, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India

来源：

ASIAN JOURNAL OF ORGANIC CHEMISTRY | 2013年 / 2卷 / 10期

关键词：

Bauhinia; dibenzo[b; f]oxepins; 2,2 '-oxybis(vinylbenzenes); ring-closing metathesis; Ullmann reaction; ULLMANN-TYPE SYNTHESIS; 1ST TOTAL-SYNTHESIS; DIARYL ETHERS; ARYL IODIDES; C-N; COPPER; DERIVATIVES; ARTOCARPOL; CATALYSTS; PHENOLS;

D O I：

10.1002/ajoc.201300141

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Dibenzo[b,f]oxepin scaffolds, which have been found in the Bauhinia plant family and have potent medicinal properties, have been prepared efficiently by a two-step protocol that involves Ullmann-type coupling and ring-closing metathesis reactions.

引用

页码：848 / 851

页数：4

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