Ruthenium-catalysed double trans-hydrosilylation of 1, 4-diarylbuta-1, 3-diynes leading to 2, 5-diarylsiloles
T Matsuda, S Kadowaki, M Murakami
Index: Matsuda, Takanori; Kadowaki, Sho; Murakami, Masahiro Chemical Communications, 2007 , # 25 p. 2627 - 2629
Full Text: HTML
Citation Number: 26
Abstract
Dihydrosilanes undergo double trans-hydrosilylation with 1,4-diarylbuta-1,3-diynes in the presence of a cationic ruthenium catalyst to afford 2,5-diarylsiloles: in particular, 9-silafluorene is a good hydrosilylating agent to produce spiro-type siloles in good yield. ... Hydrosilylation of alkynes is catalysed by various transition metal complexes, and in most cases, cis adducts are formed. 5 However, a synthesis of silole derivatives by hydrosilylation of 1,3-diynes ...
Related Articles:
One-pot synthesis and functionalization of polyynes via alkylidene carbenoids
[Luu, Thanh; Morisaki, Yasuhiro; Tykwinski, Rik R. Synthesis, 2008 , # 7 p. 1158 - 1162]