Double Morita–Baylis–Hillman (MBH) strategy; an intermolecular and a chemo selective intramolecular MBH reactions for 5/6 substituted, functionalized piperidine unit
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference59 articles.
1. For reviews on MBH see
2. Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions. A catalytic and atom economic route for carbocycles and heterocycles
3. Morita–Baylis–Hillman adduct derivatives (MBHADs): versatile reactivity in Lewis base-promoted annulation
4. Recent Advances in Organocatalytic Asymmetric Morita–Baylis–Hillman/aza-Morita–Baylis–Hillman Reactions
5. Organocatalytic enantioselective methodologies using Morita–Baylis–Hillman carbonates and acetates
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3. The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 1. Catalysis of Morita–Baylis–Hillman and Knoevenagel reactions;Chemistry of Heterocyclic Compounds;2020-02
4. Chemoselective and Highly Rate Accelerated Intramolecular Aza-Morita–Baylis–Hillman Reaction;The Journal of Organic Chemistry;2018-11-15
5. Acrylamide in Rauhut-Currier reaction; intramolecular isomerization of activated alkenes for quinolone synthesis;Tetrahedron;2017-09
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