Remarkably large remote-stereocenter-induced chromatographic differences: azulenyl 1,5-diols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Development of Highly Potent Chiral Discrimination Methods That Solve the Problems of Diastereomer Method
2. The Reaction of Some 1-Trihaloacetyl-8-methylazulenes with Base1,2
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1. Hydrogenation of Cyclic 1,3-Diones to Their 1,3-Diols Using Heterogeneous Catalysts: Toward a Facile, Robust, Scalable, and Potentially Bio-Based Route;ACS Omega;2021-01-25
2. Chemoselective formation of cyclo-aliphatic and cyclo-olefinic 1,3-diols via pressure hydrogenation of potentially biobased platform molecules using Knölker-type catalysts;Dalton Transactions;2021
3. Azulene-Modified Polysiloxanes as Gas Chromatographic Stationary Phases: Comparison of the Separatory Properties of Azulene and Naphthalene;Analytical Letters;2018-03
4. Nucleophilic Additions of Perfluoroalkyl Groups;Organic Reactions;2016-12-16
5. Influence of the Azulene Ring on the Enantioseparation of 1,5-Diols;Chromatography;2014-05-16
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