Blog

Functionalization of a Simple Dithienylethene via Palladium-Catalyzed Regioselective Direct Arylation

Hiroki Kamiya, Shuichi Yanagisawa, Satoru Hiroto, Kenichiro Itami, and Hiroshi Shinokubo

Org. Lett. 2011, ASAP. DOI: 10.1021/ol2026069

The direct arylation on the thienyl groups of a diarylethene with various aryl iodides efficiently provided arylated dithienylethenes under palladium catalysis. Unsymmetrically substituted dithienylethenes were also synthesized by this protocol. This procedure allows a rapid access to a variety of aryl-substituted dithienylethenes from a single substrate of a simple dithienylethene.

Related post

  1. Oxidative Biaryl Coupling of Thi…
  2. Casein kinase 1 family regulates…
  3. Aromatic C–H Borylation by Nicke…
  4. Selective Synthesis of [7]- and …
  5. β-Selective C–H Arylation of Pyr…
  6. Palladium-catalyzed tetraallylat…
  7. Electro-Activated Conductivity a…
  8. Dragmacidin D Synthesis of Dragmacidin D via D…

Twitter@Itami Lab

Itami Lab Facebook

最近の記事

Flickr@Itamilab

天池先輩からコーヒースープ伴夫妻からのお歳暮です!潤さん、宮村さん、ありがとうございます!!武藤さん、ビールありがとうございます!平賀大都わーいやなさん、あつしさん、ありがとうございます!!だいぶ前だけど、Stripes look #ootdHalloween lookラインを洗う時ですら格好良く。戸谷先生教育実習!imageけいしゅう、誕生日おめでとう!誕生日は英吉家!!3年生に名古屋ぼろ勝ちアピール中!!アリシア卒業おめでとう女子会!
PAGE TOP