Chiral 1-alkoxyaziridines: resolution, nitrogen inversion, stucture and diastereomeric transformations-Reference-Cited by-同舟云学术

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Chiral 1-alkoxyaziridines: resolution, nitrogen inversion, stucture and diastereomeric transformations

Published:2002-01 Issue:4 Volume:12 Page:137-140
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Kostyanovsky Remir G.,Schurig Volker,Trapp Oliver,Lyssenko Konstantin A.,Averkiev Boris B.,Kadorkina Gulnara K.,Prosyanik Alexander V.,Kostyanovsky Vasily R.

Publisher

Elsevier BV

Subject

General Chemistry

Reference41 articles.

1. Wedekind–Fock–Havinga salt Me(Et)N+(All)PhI–·CHCl3 as historically the first object for absolute asymmetric synthesis: spontaneous resolution, structure and absolute configuration

2. Nitrogen inversion in n-substituted 2,2-bis(trifluoromethyl) aziridines

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1. Unrevealing the Nitrogen Elusive Chirality of 3‐Sulfanyl and 3‐Sulfinyl N‐Tosyl Isoindolinones by ECD Spectra: An Experimental and Theoretical Investigation;Chemistry – A European Journal;2024-04-08

2. Chiral Separation by GC;Chiral Separations and Stereochemical Elucidation;2023-03-26

3. REPRODUCIBILITY OF A HOMOCHIRAL HYDROGEN-BONDED CHAIN IN CONGLOMERATE AND RACEMIC COMPOUND CRYSTALS OF THE TRIAZOLE DERIVATIVE OF 3-PYRROLINE-2-ONE;Journal of Structural Chemistry;2022-09

4. Chiral stationary phases and applications in gas chromatography;Chirality;2022-03-22

5. Experimental evidence of chalcogen bonding at oxygen;Chemical Communications;2020

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