ChemInform Abstract: A Highly Stereoselective Synthesis of a Key Intermediate (III) of 1β-Methylcarbapenems Employing the Reformatsky Reaction of 3-(2-Bromopropionyl)-2-oxazolidone Derivatives (II).

ChemInform ◽  
1988 ◽  
Vol 19 (22) ◽  
Author(s):  
Y. ITO ◽  
S. TERASHIMA
Keyword(s):  
Stereoselective Synthesis ◽  
Reformatsky Reaction ◽  
The Reformatsky Reaction

The Reformatsky Reaction with Benzalaniline

1943 ◽  
Vol 65 (11) ◽  
pp. 2255-2256 ◽  
Author(s):  
Henry Gilman ◽  
Merrill Speeter
Keyword(s):  
Reformatsky Reaction ◽  
The Reformatsky Reaction

A Short Stereoselective Synthesis of Prepiscibactin Using a SmI2-Mediated Reformatsky Reaction and Zn2+-Induced Asymmetric Thiazolidine Formation

2014 ◽  
Vol 16 (21) ◽  
pp. 5820-5823 ◽  
Author(s):  
Yuri Segade ◽  
Marcos A. Montaos ◽  
Jaime Rodríguez ◽  
Carlos Jiménez
Keyword(s):  
Stereoselective Synthesis ◽  
Reformatsky Reaction

A NEW MODIFICATION OF THE REFORMATSKY REACTION

1931 ◽  
Vol 53 (5) ◽  
pp. 1842-1846 ◽  
Author(s):  
J. A. Nieuwland ◽  
S. Florentine. Daly
Keyword(s):  
Reformatsky Reaction ◽  
The Reformatsky Reaction

Regioselective synthesis of functionalized dihydroisoquinolines from o-alkynylarylaldimines via the Reformatsky reaction

2016 ◽  
Vol 14 (41) ◽  
pp. 9896-9906 ◽  
Author(s):  
Tohasib Yusub Chaudhari ◽  
Urvashi Urvashi ◽  
Sandeep K. Ginotra ◽  
Pooja Yadav ◽  
Gulshan Kumar ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Regioselective Synthesis ◽  
Reformatsky Reaction ◽  
Novel Approach ◽  
The Reformatsky Reaction

A novel approach for the synthesis of functionalized 1,2-dihydroisoquinolines from o-alkynylarylaldimines via the Reformatsky reaction without the aid of an external Lewis acid has been described.

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