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An Alternative and Effective Catalyst in the Stereospecific Reaction of Z-1-Aryl-1-stannyl-2-silylethenes with Allyl Bromide.

✍ Scribed by Taichi Nakano; Kenji Kawai; Takanori Endoh; Shintaro Osada; Takashi Miyamoto


Publisher
John Wiley and Sons
Year
2006
Weight
15 KB
Volume
37
Category
Article
ISSN
0931-7597

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Short communication: An alternative and
✍ Taichi Nakano; Kenji Kawai; Takanori Endoh; Shintaro Osada; Takashi Miyamoto 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 104 KB 👁 1 views

The Pd(dba) 2 -catalyzed reaction of Z-1-aryl-1-(tributylstannyl)-2-(trimethylsilyl)ethenes with allyl bromide in the presence of copper(I) iodide is reported for the first time. The reaction in the presence of 0.5 mol% Pd(dba) 2 and 8 mol% CuI in dimethylformamide takes place at room temperature to

Stereospecific synthesis of a family of
✍ Fumio Sasaki; Takanori Endo; Masanori Noguchi; Kenji Kawai; Taichi Nakano 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB 👁 2 views

## Abstract Stereospecific synthesis of a family of novel (__E__)‐2‐aryl‐1‐silylalka‐1,4‐dienes or (__E__)‐4‐aryl‐5‐silylpenta‐1,2,4‐trienes via a cross‐coupling of (__Z__)‐silyl(stannyl)ethenes with allyl halides or propargyl bromide is described. In the reaction with allyl bromide, either a Pd(db