High diastereofacial selectivity in the conjugate addition of phenylmagnesium bromide to acyclic α-enones with an asymmetric carbon at the γ-position
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P2/P29910000467
Reference29 articles.
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1. ChemInform Abstract: High Diastereofacial Selectivity in the Conjugate Addition of Phenylmagnesium Bromide to Acyclic α-Enones with an Asymmetric Carbon at the γ-Position.;ChemInform;2010-08-23
2. Nucleophilic Attack on Compounds Containing CC, CO or CN Groups;PATAI'S Chemistry of Functional Groups;2009-12-15
3. Around and beyond Cram's Rule;Chemical Reviews;1999-04-28
4. Control of diastereofacial selectivity in the nucleophilic epoxidation of γ-oxygenated α,β-unsaturated sulfones;J. Chem. Soc., Perkin Trans. 1;1995
5. Addition of Organomagnesium Compounds to Carbonyl Groups;Organomagnesium Methods in Organic Synthesis;1995
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