Secondary alcohol hemiacetal formation: An in situ carbonyl activation strategy
A simple strategy was studied for the reversible nucleophilic addition of secondary alcohols to carbonyl-based receptors to form hemiacetals. It involves the in situ binding of neighboring Bronsted and Lewis acids activators. The addition reaction was suc
You, Lei,Anslyn, Eric V.
supporting information; experimental part
p. 5126 - 5129
(2009/12/28)
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