Ionic and Organometallic Reductions with N-Heterocyclic Carbene Boranes

Surgical reduction: N‐Heterocyclic carbene–borane complexes such as depicted are neutral, organic soluble analogues of borohydride anions with a weak hydridic character, compatible with organometallic catalysis. They are applicable for surgical reductions in complex, multifunctional molecules.

Saved in:

Bibliographic Details
Published in:	Chemistry : a European journal Vol. 15; no. 47; pp. 12937 - 12940
Main Authors:	Chu, Qianli, Makhlouf Brahmi, Malika, Solovyev, Andrey, Ueng, Shau-Hua, Curran, Dennis P., Malacria, Max, Fensterbank, Louis, Lacôte, Emmanuel
Format:	Journal Article
Language:	English
Published:	Weinheim WILEY-VCH Verlag 07-12-2009 WILEY‐VCH Verlag
Subjects:	aromatic substitution boranes N-heterocyclic carbenes palladium reduction
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	Surgical reduction: N‐Heterocyclic carbene–borane complexes such as depicted are neutral, organic soluble analogues of borohydride anions with a weak hydridic character, compatible with organometallic catalysis. They are applicable for surgical reductions in complex, multifunctional molecules.
Bibliography:	istex:0E62468BBF831BC483696AB65515B61A9F687304 ark:/67375/WNG-QM03SQ69-4 CNRS UPMC ArticleID:CHEM200902450 ANR - No. BLAN0309 IUF French Agence Nationale de la Recherche National Science Foundation ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0947-6539 1521-3765
DOI:	10.1002/chem.200902450