A stereoselective formal total synthesis of (+)-hyperaspine via a tandem aza-Michael reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Hyperaspine, a new 3-oxaquinolizidine alkaloid from Hyperaspis campestris (Coleoptera: Coccinellidae)
2. Preparation of syn-δ-Hydroxy-β-amino Esters via an Intramolecular Hydrogen Bond Directed Diastereoselective Hydrogenation. Total Synthesis of (3S,4aS,6R,8S)-Hyperaspine
3. Synthesis and Absolute Configuration of Hyperaspine, an Alkaloid of the LadybirdHyperaspis campestris
4. A Six-Step Asymmetric Synthesis of (+)-Hyperaspine
5. Stereospecific total synthesis of (−)-8-epi-hyperaspine
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1. Bicyclic 6-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 1:0;Comprehensive Heterocyclic Chemistry IV;2022
2. The endo-aza-Michael addition in the synthesis of piperidines and pyrrolidines;Organic & Biomolecular Chemistry;2020
3. Stereoselective Synthesis of Pyrido- and Pyrrolo[1,2-c][1,3]oxazin-1-ones via a Nucleophilic Addition–Cyclization Process of N,O-Acetal with Ynamides;The Journal of Organic Chemistry;2018-12-21
4. Lipase immobilization on hyroxypropyl methyl cellulose support and its applications for chemo-selective synthesis of β-amino ester compounds;Process Biochemistry;2016-10
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