Issue 34, 2013

Palladium-catalyzed cleavage of the Me–Si bond in ortho-trimethylsilyl aryltriflates: synthesis of benzosilole derivatives from ortho-trimethylsilyl aryltriflates and alkynes

Abstract

An efficient Pd-catalyzed cleavage of the Me–Si bond in ortho-trimethylsilyl aryltriflates was realized and synthetically applied. Most of the commercially available ortho-trimethylsilyl aryltriflates could undergo the Pd-catalyzed intermolecular coupling with alkynes via cleavage of the Me–Si bond, which represents a new reaction pattern of ortho-trimethylsilyl aryltriflates. Potassium bromide (KBr) was found effective for this process. A variety of benzosilole derivatives were thus generated in high yields.

Graphical abstract: Palladium-catalyzed cleavage of the Me–Si bond in ortho-trimethylsilyl aryltriflates: synthesis of benzosilole derivatives from ortho-trimethylsilyl aryltriflates and alkynes

Supplementary files

Article information

Article type
Communication
Submitted
13 Jun 2013
Accepted
25 Jun 2013
First published
26 Jun 2013

RSC Adv., 2013,3, 14273-14276

Palladium-catalyzed cleavage of the Me–Si bond in ortho-trimethylsilyl aryltriflates: synthesis of benzosilole derivatives from ortho-trimethylsilyl aryltriflates and alkynes

T. Meng, K. Ouyang and Z. Xi, RSC Adv., 2013, 3, 14273 DOI: 10.1039/C3RA42910E

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