Dependence of the Reactivities of Titanium Enolates on How They Are Generated:  Diastereoselective Coupling of Phenylacetic Acid Esters Using Titanium Tetrachloride

1996 ◽  
Vol 61 (8) ◽  
pp. 2809-2812 ◽  
Author(s):  
Yoshihiro Matsumura ◽  
Maiko Nishimura ◽  
Hiroyuki Hiu ◽  
Mitsuaki Watanabe ◽  
Naoki Kise
Keyword(s):  
Titanium Tetrachloride ◽  
Phenylacetic Acid ◽  
Titanium Enolates ◽  
Acid Esters

Directed Iridium‐Catalyzed Hydrogen Isotope Exchange Reactions of Phenylacetic Acid Esters and Amides

2019 ◽  
Vol 25 (26) ◽  
pp. 6517-6522 ◽  
Author(s):  
Mégane Valero ◽  
Daniel Becker ◽  
Kristof Jess ◽  
Remo Weck ◽  
Jens Atzrodt ◽  
...  
Keyword(s):  
Hydrogen Isotope ◽  
Isotope Exchange ◽  
Phenylacetic Acid ◽  
Exchange Reactions ◽  
Hydrogen Isotope Exchange ◽  
Acid Esters

Stereoselective Synthesis of 3-azabicyclo[3,3,1]Nonan-9α-yl α-(cyclopentyl-1-ene)-α-hydroxy-α-phenylacetate Hydrochloride

2005 ◽  
Vol 2005 (5) ◽  
pp. 322-323 ◽  
Author(s):  
He Liu ◽  
Xiang-Yu Han ◽  
Bo-Hua Zhong ◽  
Ke-Liang Liu
Keyword(s):  
Mandelic Acid ◽  
Phenylacetic Acid ◽  
Stereoselective Synthesis ◽  
Enantiomeric Excess ◽  
Starting Material ◽  
Sterically Hindered ◽  
Acid Esters

The isomers of α-(cyclopentyl-1-ene)-α-hydroxy-α-phenylacetic acid esters derived from 3-azabicyclo[3,3,1]nonan-9α-ol ((R)-1 and (S)-1) were obtained in high enantiomeric excess by effective stereoselective synthesis from the chiral starting material, (S) or (R)-mandelic acid using pivaldehyde as a sterically hindered reagent

Mono- and bis(aminomethyl)phenylacetic acid esters as short-acting antiarrhythmic agents. 2

1993 ◽  
Vol 36 (17) ◽  
pp. 2494-2498 ◽  
Author(s):  
Robert J. Chorvat ◽  
Lawrence A. Black ◽  
Vasant V. Ranade ◽  
Cynthia Barcelon-Yang ◽  
David M. Stout ◽  
...  
Keyword(s):  
Phenylacetic Acid ◽  
Antiarrhythmic Agents ◽  
Short Acting ◽  
Acid Esters
Sign in / Sign up

Export Citation Format

Share Document