Hydrochloride of chiral piperazine as a chiral proton source
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference65 articles.
1. Asymmetric Synthesis of ?-Substituted Ketones by Metalation and Alkylation of Chiral Hydrazones
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4. Chiral α,ω-dioxy-carbanions from 1,3-propanediol and 1,4-butanediol by sparteine-assisted deprotonation. Enantioselective synthesis of 1,3- and 1,4-diols, (R)-pantolactone, and a cyclopropane.
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1. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives;Comprehensive Organic Transformations;2018-02-28
2. Diamine Ligands for Asymmetric Catalysis: Facile Synthesis of C2-Symmetric Piperazines from Seebach’s Oxazolidinone;Synlett;2014-07-08
3. C2-Symmetric hemiaminal ethers and diamines: new ligands for copper-catalyzed desymmetrization of meso-1,2-diols and asymmetric Henry reactions;Tetrahedron: Asymmetry;2013-11
4. One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines;Organic & Biomolecular Chemistry;2012
5. ChemInform Abstract: Hydrochloride of Chiral Piperazine as a Chiral Proton Source.;ChemInform;2010-08-20
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