๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Allylic Alcohols by an Enantioselective Isomerization/Transfer Hydrogenation Mechanism

โœ Scribed by Ruoqiu Wu; Marie G. Beauchamps; Joseph M. Laquidara; Prof. John R. Sowa Jr.

Book ID
111999590
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
403 KB
Volume
124
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Ruthenium-Catalyzed Reduction of Allylic
Ruthenium-Catalyzed Reduction of Allylic Alcohols: An Efficient Isomerization/Transfer Hydrogenation Tandem Process.
โœ Victorio Cadierno; Javier Francos; Jose Gimeno; Noel Nebra ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons โš– 27 KB ๐Ÿ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Highly Efficient Redox Isomerization of
Highly Efficient Redox Isomerization of Allylic Alcohols and Transfer Hydrogenation of Ketones and Aldehydes Catalyzed by Ruthenium Complexes
โœ Pei Nian Liu; Kun Dong Ju; Chak Po Lau ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 183 KB ๐Ÿ‘ 2 views

## Abstract A dicationic dichloroโ€bipyridineโ€ruthenium complex shows very high catalytic activity in redox isomerization of allylic alcohols but a relatively low one in transfer hydrogenation of ketones; surprisingly, the analogous dimethylโ€bipyridineโ€ruthenium complex shows reverse catalytic activ

ChemInform Abstract: Highly Efficient Re
ChemInform Abstract: Highly Efficient Redox Isomerization of Allylic Alcohols and Transfer Hydrogenation of Ketones and Aldehydes Catalyzed by Ruthenium Complexes.
โœ Pei Nian Liu; Kun Dong Ju; Chak Po Lau ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons โš– 63 KB ๐Ÿ‘ 2 views

## Abstract A Ru(II)โ€”dichlorobipyridine complex (Ia) efficiently catalyzes the redox isomerization of terminal and internal allylic alcohols to give the corresponding ketones, e.g. (III), (V) or (VII), in high to excellent conversion.