Reactivity of Organocerium Compounds with Allyl Alcohols
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo981130h
Reference31 articles.
1. Cerium chloride (III) promoted nucleophilic addition of organolithium reagents to α-diphenylphosphinoyl ketones. An efficient method for the synthesis of horner-wittig intermediates
2. Cerium(III) chloride mediated Michael addition of RMgX to nitroenes: A very efficient access to complex nitroalkanes
3. Cerium(III) Chloride Promoted Nucleophilic Addition of Organolithium Reagents toα-Alkyl-β-Ketophosphine Oxides: A New Protocol for the Synthesis of Stereochemically Defined Trisubstituted Olefins
4. A Stereoselective Synthesis of (E)-α, β-Unsaturated Ketones Involving the Reactions of Organocerium Reagents with Secondary β-Enamino Ketones
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1. Organocerium reagents;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21
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3. Mechanistic study on a unique SN2′-type reaction of allylic alcohols with organolithium reagent accelerated by a proximal trifluoromethyl group;Journal of Fluorine Chemistry;2015-11
4. Alkenenitrile Transmissive Olefination: Synthesis of the Putative Lignan “Morinol I”;European Journal of Organic Chemistry;2011-10-28
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