Paper
Asymmetric Synthesis of (2S) - 2 - Brom -1 -(6' - methoxy - 2' - naphthy 1)propan -1 - one
Published 1999 · H. Ai
Chinese Journal of Organic Chemistry
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Abstract
(2S) - 2 - Brom - 1 - (6' - methoxy - 2' - naphthyl)propan - 1 - one was systhsized by acetalization, asymmetric bromination, hydrolysis of 6 - methoxy - 2 - propionyl naphthalene using( 2R, 3 R ) -dimethyl tartrate as chiral auxiary,cupricbromide as the brominating agent with 94% total yield.
Study Snapshot
This study demonstrates a 94% total yield for the asymmetric synthesis of (2S) - 2 - Brom -1 - (6'-methoxy - 2' - naphthyl)propan -1 - one using chiral auxiary and cupric bromide
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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