“Doubly enantiophobic” behavior during crystallization of racemic 1,5-dihydro-2H-pyrrol-2-one thioether-Reference-Cited by-同舟云学术

“Doubly enantiophobic” behavior during crystallization of racemic 1,5-dihydro-2H-pyrrol-2-one thioether

Published:2018 Issue:23 Volume:20 Page:3218-3227
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Lodochnikova Olga A.¹²³⁴⁵^ORCID,Zaripova Aigul R.¹²³⁴⁵,Fayzullin Robert R.¹²³⁴^ORCID,Samigullina Aida I.¹²³⁴^ORCID,Vandyukova Irina I.¹²³⁴,Potapova Lubov N.⁵⁶⁷⁴,Kurbangalieva Almira R.⁵⁶⁷⁴^ORCID

Affiliation:

1. Arbuzov Institute of Organic and Physical Chemistry

2. FRC Kazan Scientific Center of RAS

3. Kazan 420088

4. Russian Federation

5. A.M. Butlerov Institute of Chemistry

6. Kazan Federal University

7. Kazan 420008

Abstract

One racemate forms two conglomerates and no racemic compound.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CE/C8CE00369F

Reference43 articles.

1. J. Jacques , A.Collet and S. H.Wilen , Enantiomers, Racemates and Resolutions , Krieger Publishing Company , 1994

2. Processes To Separate Enantiomers

3. Spontaneous resolution, whence and whither: from enantiomorphic solids to chiral liquid crystals, monolayers and macro- and supra-molecular polymers and assemblies

4. Molecular packing modes. Carboxylic acids

5. Achiral molecules in non-centrosymmetric space groups

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