Volume 31, Issue 16
Organoelement Compounds
Full Access

ChemInform Abstract: Palladium-Catalyzed Borylation of Aryl Halides or Triflates with Dialkoxyborane: A Novel and Facile Synthetic Route to Arylboronates.

Miki Murata

Miki Murata

Dep. Mater. Sci., Kitami Inst. Technol., Koen, Kitami 090, Japan

Search for more papers by this author
Takashi Oyama

Takashi Oyama

Dep. Mater. Sci., Kitami Inst. Technol., Koen, Kitami 090, Japan

Search for more papers by this author
Shinji Watanabe

Shinji Watanabe

Dep. Mater. Sci., Kitami Inst. Technol., Koen, Kitami 090, Japan

Search for more papers by this author
Yuzuru Masuda

Yuzuru Masuda

Dep. Mater. Sci., Kitami Inst. Technol., Koen, Kitami 090, Japan

Search for more papers by this author
First published: 09 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The previously reported title method is successfully extended to aryl sulfonates and thus represents a new route to pinacolboronates of type (III) (17 examples). Generally, aryl iodides exhibit higher reactivity than aryl bromides or sulfonates, but the use of sulfonates has some advantages, in part due to the easy availability from phenols. The present method tolerates various functional groups such as CO2Et, COMe, CN, and NHAc.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.