Dibal-h cas no

Al 2 O 3 , AmO , AmO 2 , Sb 2 O 3 , Sb 2 O 5 , As 2 O 3 , As 2 O 5 , BaO , BeO , Bi 2 O 3 , BiOCl , B 2 O 3 , Br 2 O , CO 2 , CO , CeO 2 , ClO 2 , ClO 3 , Cl 2 O 7 , Cl 2 O , Cr 2 O 3 , CrO 2 , CrO 3 , CoO , Cu 2 O , CuO , Cm 2 O 3 , CmO 2 , Dy 2 O 3 , Er 2 O 3 , Eu 2 O 3 , OF 2 , O 2 F 2 , Fr 2 O , Gd 2 O 3 , Ga 2 O 3 , GeO 2 , Au 2 O 3 , HfO 2 , Ho 2 O 3 , In 2 O , In 2 O 3 , I 2 O 5 , IrO 2 , FeO , Fe 3 O 4 , Fe 2 O 3 , La 2 O 3 , PbO , PbO 2 , Li 2 O , MgO , K 2 O , Rb 2 O , Na 2 O , SrO , TeO 2 , UO 2

DIBAL is useful in organic synthesis for a variety of reductions, including converting carboxylic acids , their derivatives, and nitriles to aldehydes . DIBAL efficiently reduces α-β unsaturated esters to the corresponding allylic alcohol. [4] By contrast, LiAlH 4 reduces esters and acyl chlorides to primary alcohols , and nitriles to primary amines [use Feiser work-up procedure]. DIBAL reacts slowly with electron-poor compounds, and more quickly with electron-rich compounds. Thus, it is an electrophilic reducing agent whereas LiAlH 4 can be thought of as a nucleophilic reducing agent.

Dibal-h cas no

dibal-h cas no

Media:



http://buy-steroids.org