Wohl-Ziegler reaction
(organic chemistry) The tetrachloro derivative of hydroquinone 2,3,5,6-tetrachlorobenzene-1,4-diol
(obsolete, chemistry) Created by the destructive distillation of wood.
(chemistry) A chemical reaction that involves the allylic or benzylic bromination of hydrocarbons using an N-bromoimide and a radical initiator.
plural of Schleis
合成では、N-ブロモイミドとラジカル開始剤によるアリル位またはベンジル位の臭化反応を用いて、アルケンのアリル位に選択的に臭素を導入した。
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