Stereoselective Bromination of Dehydroamino Acids with Controllable Retention or Inversion of Olefin Configuration
Dehydroamino acids react with brominating reagents to produce syn-α-bromo imines as the major products, which undergo tautomerization to mixtures of the diastereomeric (E)- and (Z)-β-bromo-α,β-dehydroamino acids upon treatment with base.Herein, we examine
Coleman, Robert S.
p. 4452 - 4461
(2007/10/02)
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