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Chiral Phosphine (chiral + phosphine)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

Chiral Phosphine,Olefin Ligands in the Rhodium-Catalyzed Asymmetric 1,4-Addition Reactions.

CHEMINFORM, Issue 24 2007
Wei-Liang Duan
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. [source]

Chiral Phosphine,Olefin Bidentate Ligands in Asymmetric Catalysis: Rhodium-Catalyzed Asymmetric 1,4-Addition of Aryl Boronic Acids to Maleimides.

CHEMINFORM, Issue 48 2005
Ryo Shintani
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

ChemInform Abstract: Novel Chiral Phosphine,Oxazinane Ligands in Palladium-Catalyzed Asymmetric Allylic Alkylation.

CHEMINFORM, Issue 41 2001
Takashi Mino
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. [source]

A Promising New Catalyst Family for Enantioselective Cycloadditions Involving Allenes and Imines: Chiral Phosphines with Transition Metal,CH2,P: Linkages.

CHEMINFORM, Issue 50 2006
Alexander Scherer
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. [source]

Catalytic Asymmetric Intramolecular Cascade Reaction for the Construction of Functionalized Benzobicyclo[4.3.0] Skeletons.

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 11-12 2010
Remote Control of Enantioselectivity
Abstract A catalytic asymmetric version of the intramolecular ylide annulation has been developed which affords high ee values and diastereoselectivities and which further shows that spirobiindane-based chiral phosphines can be excellent organocatalysts. Both optically active benzobicyclo[4.3.0] compounds 2 and 2, with three continuous stereogenic centers could be obtained as major products selectively under neutral and mild conditions just by a choice of an additive. [source]