Palladium-Catalyzed Annulation of Internal Alkynes: Direct Access to π-Conjugated Ullazines

被引：36

作者：

Wan, Danyang ^{[1
,2
]}

Li, Xiaoyu ^{[1
,2
]}

Jiang, Ruyong ^{[1
,2
]}

Feng, Boya ^{[1
,2
]}

Lan, Jingbo ^{[1
,2
]}

Wang, Ruilin ^{[3
]}

You, Jingsong ^{[1
,2
]}

机构：

[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, 29 Wangjiang Rd, Chengdu 610064, Peoples R China

[2] Sichuan Univ, West China Med Sch, State Key Lab Biotherapy, 29 Wangjiang Rd, Chengdu 610064, Peoples R China

[3] Sichuan Univ, Coll Mat Sci & Engn, 29 Wangjiang Rd, Chengdu 610064, Peoples R China

来源：

ORGANIC LETTERS | 2016年 / 18卷 / 12期

关键词：

C-H ACTIVATION; OXIDATIVE ANNULATION; SOLAR-CELLS; HYDROCARBONS; HETEROARENES; MOLECULES; ARYLATION; DESIGN; BONDS;

D O I：

10.1021/acs.orglett.6b01182

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A palladium-catalyzed cyclization reaction of 1-(2,6-dibromophenyl)-1H-pyrroles with alkynes has been developed to construct various p-conjugated indolizino[6,5,4,3-ija]quinolones (ullazines) with a reactive functional group tolerance. As illustrative examples, three new ullazine-based sensitizers are synthesized, and the performance of these dyes is examined in DSSC devices, which demonstrates the potential of direct C-H functionalization in the construction of organic optoelectronic materials.

引用

页码：2876 / 2879

页数：4

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