Efficient Stereoselective Synthesis and Optical Properties of Heteroleptic Square‐Planar Platinum(II) Complexes with Bidentate Iminopyrrolyl Ligands

2020 ◽  
Vol 2020 (41) ◽  
pp. 3959-3966
Author(s):  
Ryo Inoue ◽  
Yasuhiro Morisaki
2019 ◽  
Vol 48 (27) ◽  
pp. 10138-10144
Author(s):  
Yutaro Goto ◽  
Yutaka Watanabe ◽  
Aoki Noboriguchi ◽  
Jun Yoshida ◽  
Shigeki Mori ◽  
...  

Tetranuclear Pd(ii)complexes were synthesized according to the molecular tectonics approach. A focus was how the elongation of a molecular axis affected the chiro-optical properties of a molecule with axial chirality.


1991 ◽  
Vol 69 (7) ◽  
pp. 1100-1106 ◽  
Author(s):  
David Miller ◽  
François Bilodeau ◽  
Robert H. Burnell

Two related stereoselective syntheses of 3,7-dimethylnonadecane, a sex pheromone of the alfalfa leafminer, are described to show that pulegone can serve as a useful starting material for the preparation of chiral aliphatic isoprenoid compounds. The schemes are designed to place the stereogenic center of pulegone at C.3 in one synthesis and at C.7 in the other so that the optical properties of the products can be compared with one another and with the values calculated using Brewster's rules. Key words: chiral hydrocarbons, stereoselective synthesis, pheromone, Agromyza frontella.


1992 ◽  
Author(s):  
Zakya H. Kafafi ◽  
James R. Lindle ◽  
Steven R. Flom ◽  
Richard G. S. Pong ◽  
C. S. Weisbecker ◽  
...  

2001 ◽  
Vol 121 (1-3) ◽  
pp. 1491-1492 ◽  
Author(s):  
Chuluo Yang ◽  
Jingui Qin ◽  
Qiguang Yang ◽  
Jinhai Si ◽  
Shoubai Wang ◽  
...  

2011 ◽  
Vol 13 (3) ◽  
pp. 12-17 ◽  
Author(s):  
Donka Tasheva ◽  
Sonya Zareva

Tert-butyl esters of 2,3-diaryl-3-arylaminopropanoic acids - stereoselective synthesis, isolation, spectroscopic and structural elucidation A series of seven substituted tert-butyl esters of 2,3-diaryl-3-arylaminopropanoic acids has been synthesized, isolated, spectroscopically and structurally elucidated. An influence of the substituents on the spectroscopic characteristics and conformations is discussed using the data of the linear-polarized IR- (IR-LD), UV-spectroscopy and 1H-NMR. Theoretical quantum chemical calculations are carried out, with a view to explaining and supporting the experimental optical properties and the electronic structure. The stereoselective synthesis of the corresponding diastereoisomers is optimized, thus giving good yields (62-72%) and purity of the compounds


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