Chiral cyclic β-amino esters. Part I: Synthesis by diastereospecific alkylation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Total synthesis of (.+-.)-lythrancepine II and (.+-.)-lythrancepine III
2. Enantioselective synthesis of (−)-gephyrotoxine 223AB [(3R,5R,9R)-3-butyl-5-propyloctahydroindolizine]
3. Aza-annulation as a route to hydroxylated alkaloid lipids. The synthesis of (±)-prosopinine
4. A Novel Asymmetric Route to Chiral, Nonracemic cis-2,6-Disubstituted Piperidines. Synthesis of (+)-Pinidinone and (+)-Monomorine
5. Enantioselective synthesis of (−)-indolizidine 239AB [(3R,5S,8aR)-3-butyl-5-(3-hydroxypropyl)-octahydroindolizine]
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1. A Direct, Versatile, and Chemoselective Synthesis of Vinylogous Bis- and Monourethanes/amides and β-Keto Esters by Aza-Knoevenagel-Type Reactions of Tertiary Amides with Enolates;European Journal of Organic Chemistry;2017-01-18
2. Simple Indolizidine and Quinolizidine Alkaloids;The Alkaloids: Chemistry and Biology;2016
3. Asymmetric syntheses of dihydroxyhomoprolines via doubly diastereoselective lithium amide conjugate addition reactions;Tetrahedron;2013-10
4. Total Synthesis of Indolizidine (+)-223A;European Journal of Organic Chemistry;2011-12-07
5. ChemInform Abstract: Chiral Cyclic β-Amino Esters. Part 1. Synthesis by Diastereospecific Alkylation.;ChemInform;2010-06-23
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