Stereoselective synthesis of a new optically active phosphinoacyloxazolidinone via enantioselective hydrogenation

1998 ◽  
pp. 533-534 ◽  
Author(s):  
Pierre Le Gendre ◽  
François Jérôme ◽  
Christian Bruneau ◽  
Pierre H. Dixneuf
Keyword(s):  
Stereoselective Synthesis ◽  
Enantioselective Hydrogenation ◽  
Optically Active

Stereoselective synthesis of optically active cyclopenta[c]pyridines and tetrahydropyridines

2012 ◽  
Vol 23 (9) ◽  
pp. 662-669 ◽  
Author(s):  
Serdar Sezer ◽  
Yasemin Gümrükçü ◽  
İrem Bakırcı ◽  
M. Yağız Ünver ◽  
Cihangir Tanyeli
Keyword(s):  
Stereoselective Synthesis ◽  
Optically Active

Asymmetrische Katalysen, 25 [1]. C5H5Mn(CO)2-Komplexe von optisch aktiven Chelatphosphanen als einzähnige Liganden in der enantioselektiven Katalyse / Asymmetric Catalyses, 25 [1]. C5H5Mn(CO)2 Complexes of Optically Active Chelate Phosphanes as Monodentate Ligands in Enantioselective Catalysis

1985 ◽  
Vol 40 (10) ◽  
pp. 1243-1249 ◽  
Author(s):  
Henri Brunner ◽  
Alfons Knott
Keyword(s):  
Cinnamic Acid ◽  
Enantioselective Hydrogenation ◽  
Optically Active ◽  
Enantioselective Catalysis ◽  
Dinuclear Complexes ◽  
Bidentate Ligands ◽  
Monodentate Ligand ◽  
Mononuclear Complexes ◽  
Monodentate Ligands

The chelate phosphanes Diphos, Diop, and Norphos were reacted with C5H5Mn(CO)2THF and CH3C5H4Mn(CO)2THF to give mononuclear complexes, containing the phosphanes as unidentate or as bidentate ligands, and dinuclear complexes, containing bridging phosphane ligands. In C5H5Mn(CO)2Diop one of the two P(C6H5)2 groups of Diop is coordinated to the C5H5Mn(CO)2 fragment; the uncoordinated P(C6H5)2 group makes it a monodentate ligand. C5H5Mn(CO)2Diop together with [Rh(cod)Cl]2 was used as an in situ catalyst in the enantioselective hydrogenation of (Z)-a-[N -acetam ino]cinnamic acid (78.4% ee) and in the enantioselective hydrosilylation of acetophenone with diphenylsilane (6.7% ee).

A new approach to the stereoselective synthesis of trans-3-carbamoyl-β-lactam moieties

2017 ◽  
Vol 41 (6) ◽  
pp. 2479-2489 ◽  
Author(s):  
Anna Zakaszewska ◽  
Ewelina Najda-Mocarska ◽  
Sławomir Makowiec
Keyword(s):  
Stereoselective Synthesis ◽  
Optically Active ◽  
Thermal Generation ◽  
New Approach

Optically active 1,4-disubstituted-3-carbamoyl-azetidinones are synthesized from 5-[(N-arylamino)(hydroxyl)methylene]-2,2-dimethyl-1,3-dioxa-4,6-diones and chiral aldimines via thermal generation of carbamoyl ketenes and subsequent [2+2] cycloaddition.

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