Literature DB >> 15915521

Quasienantiomers and quasiracemates: new tools for identification, analysis, separation, and synthesis of enantiomers.

Qisheng Zhang1, Dennis P Curran.   

Abstract

The old adage "never mix pure organic compounds" holds in spades for enantiomers. After going to all the trouble to make enantiopure molecules, who in their right mind would ever mix them to make a racemate? Quasienantiomers are almost enantiomers, but not quite. Yet unlike enantiomers, the interest is not so much in separating them but in mixing them to make quasiracemates. This backwards thinking opens new possibilities for identification, analysis, separation and synthesis of enantiomers. A short history is provided, the terms are defined and illustrated, and recent applications of quasienantiomers, quasiracemates and related species are reviewed.

Mesh:

Year:  2005        PMID: 15915521     DOI: 10.1002/chem.200500076

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  13 in total

1.  Fluorous Mixture Synthesis of Four Stereoisomers of the C21-C40 Fragment of Tetrafibricin.

Authors:  Kai Zhang; Dennis P Curran
Journal:  Synlett       Date:  2010-03-01       Impact factor: 2.454

2.  Assignment of the structure of petrocortyne A by mixture syntheses of four candidate stereoisomers.

Authors:  Bin Sui; Edmund A-H Yeh; Dennis P Curran
Journal:  J Org Chem       Date:  2010-05-07       Impact factor: 4.354

3.  Bare-minimum fluorous mixture synthesis of a stereoisomer library of 4,8,12-trimethylnonadecanols and predictions of NMR spectra of saturated oligoisoprenoid stereoisomers.

Authors:  Edmund A-H Yeh; Eveline Kumli; Krishnan Damodaran; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2013-01-18       Impact factor: 15.419

4.  Fluorous mixture synthesis of two libraries with hydantoin-, and benzodiazepinedione-fused heterocyclic scaffolds.

Authors:  Wei Zhang; Yimin Lu; Christine Hiu-Tung Chen; Lu Zeng; Daniel B Kassel
Journal:  J Comb Chem       Date:  2006 Sep-Oct

5.  Synthesis and spectroscopic analysis of a stereoisomer library of the phytophthora mating hormone α1 and derived bis-Mosher esters.

Authors:  Reena Bajpai; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2011-11-28       Impact factor: 15.419

6.  Catalytic parallel kinetic resolution under homogeneous conditions.

Authors:  Trisha A Duffey; James A Mackay; Edwin Vedejs
Journal:  J Org Chem       Date:  2010-07-16       Impact factor: 4.354

7.  Minimal fluorous tagging strategy that enables the synthesis of the complete stereoisomer library of SCH725674 macrolactones.

Authors:  Jared D Moretti; Xiao Wang; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2012-05-01       Impact factor: 15.419

8.  Comparison of the Relative Reactivities of the Triisopropylsilyl Group With Two Fluorous Analogs.

Authors:  Amador Garcia Sancho; Xiao Wang; Bin Sui; Dennis Curran
Journal:  Adv Synth Catal       Date:  2009-05-01       Impact factor: 5.837

9.  A "shortcut" Mosher ester method to assign configurations of stereocenters in nearly symmetric environments. Fluorous mixture synthesis and structure assignment of petrocortyne A.

Authors:  Dennis P Curran; Bin Sui
Journal:  J Am Chem Soc       Date:  2009-04-22       Impact factor: 15.419

10.  Fluorous Synthesis of Hydantoin-, Piperazinedione-, and Benzodiazepinedione-Fused Tricyclic and Tetracyclic Ring Systems.

Authors:  Wei Zhang; Yimin Lu; Christine Hiu-Tung Chen; Dennis P Curran; Steven Geib
Journal:  European J Org Chem       Date:  2006
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.