Blog

Palladium-Catalyzed C–H and C–N Arylation of Aminothiazoles with Arylboronic Acids

Takahiro N. Uehara, Junichiro Yamaguchi and Kenichiro Itami Asian J. Org. Chem2013 DOI: 10.1002/ajoc.201300172

(Dedicated to Professor Teruaki Mukaiyama on the occasion of the 40th anniversary of the Mukaiyama aldol reaction.)

 

C–H and C–N Arylation

A C4-selective C–H arylation of 2-aminothiazoles with arylboronic acids takes place under the influence of Pd(OAc)2/phen/TEMPO/LiBF4 in air. During this study, a Pd-catalyzed C–N cleavage/arylation of 2-aminobenzothiazoles with arylboronic acids has been discovered. bipy=2,2-bipyridyl; TEMPO=2,2,6,6-tetramethylpiperidin-1-oxyl.

 

Related post

  1. Programmable Synthesis of Multip…
  2. Rapid Access to Kinase Inhibitor…
  3. [9]Cycloparaphenylene: Nickel-Me…
  4. A General Catalyst for the b-Sel…
  5. Synthesis of Sterically Hindered…
  6. Aziridinofullerene: A Versatile …
  7. Flexible Reaction Pocket on Bulk…
  8. CH Alkenylation of Azoles with E…

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