74685-32-8

Downstream Products

• 41927-29-1 (S)-2-methyl-4-phenyl-1-butyric acid 
• 80651-37-2 (R)-(-)-2-methyl-4-phenylbutyric acid 
• 168038-38-8 (R)-(-)-3-(2-phenylethyl)cyclohexanone 
• 1204587-61-0 benzyl 4-oxo-2-phenethyl-3,4-dihydropyridine-1(2H)-carboxylate 
• 14097-24-6 (S)-1,3-diphenylpropanol 
• 1182228-47-2 (S)-(+)-(2-(cyclohex-2-en-1-yl)ethyl)benzene 
• 1241732-15-9 (R)-(2-(cyclohept-2-enyl)ethyl)benzene 
• 1182228-56-3 (S)-(2-(cyclohept-2-enyl)ethyl)benzene 
• 1029010-55-6 2-{[(2R)-2,4-diphenylbutyl]sulfonyl}pyridine 

Relevant academic research and scientific papers

METHODS FOR PREPARING DIORGANOZINC COMPOUNDS

There are provided methods for preparing the diorganozmc compounds of formula R2Zn (I or Ia), where R is a defined organic radical, and the two R groups can be the same or different The starting material is the zinc compound ZnX2 (II) or R2ZnX (IIa), where X is a defined anion and R2 is a defined organic radical. The zinc reagent of type II is combined with a Grignard reagent and also, when X is Cl or Br, with an alkali metal reagent (VI) to form the diorganozinc product (I or Ia). Also provided are methods for preparing the zinc alcoholates of formula Zn(OR1)2 by reaction of ZnX2, where X = Cl or Br, with an alkali metal reagent of the formula MOR1, where M = Na or K, and where R1 is a defined organic radical.