## Abstract The palladium‐catalyzed cross‐coupling reaction of organogold(I) reagents (alkyl, alkenyl, aryl, and alkynyl) with organic electrophiles, such as aryl and alkenyl halides, aryl triflates, benzyl bromide, and benzoyl chloride is reported. The reaction takes place, under palladium catalys
✦ LIBER ✦
Palladium-Catalyzed Cross-Coupling of Aryl Electrophiles with Dimethylalkynylaluminum Reagents.
✍ Scribed by Baomin Wang; Martine Bonin; Laurent Micouin
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 274 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Palladium-Catalyzed Cross-Coupling React
✍
Miguel Peña-López; Miguel Ayán-Varela; Luis A. Sarandeses; José Pérez Sestelo
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 218 KB
ChemInform Abstract: Palladium-Catalyzed
✍
Miguel Pena-Lopez; Miguel Ayan-Varela; Luis A. Sarandeses; Jose Perez Sestelo
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 49 KB
👁 1 views
Palladium-Catalyzed Cross-Coupling React
✍
Mingxing Qian; Ei-ichi Negishi
📂
Article
📅
2005
🏛
John Wiley and Sons
⚖ 18 KB
Palladium-Catalyzed Cross-Coupling Invol
✍
Takumichi Sugihara
📂
Article
📅
2003
🏛
John Wiley and Sons
⚖ 72 KB
👁 1 views
Low Temperature Studies of Iron-Catalyze
✍
Jonatan Kleimark; Per-Fredrik Larsson; Parisa Emamy; Anna Hedström; Per-Ola Norr
📂
Article
📅
2012
🏛
John Wiley and Sons
🌐
English
⚖ 441 KB
👁 2 views
## Abstract The title reaction has been studied under low temperature conditions. Coupling with active substrates can be done even at dry ice temperature. Initial rate studies at −25 °C indicate that high concentrations of any reagent can lead to either complete or partial catalyst deactivation. Un
Nickel-Catalyzed Cross-Coupling of Aryl
✍
Volker P. W. Böhm; Thomas Weskamp; Christian W. K. Gstöttmayr; Wolfgang A. Herrm
📂
Article
📅
2000
🏛
John Wiley and Sons
🌐
English
⚖ 102 KB
👁 2 views