Literature DB >> 26364568

Absolute Configuration Determination of Azulenyl Diols Isolated From Asymmetric Pinacol Coupling.

Eugenia Andreea Dragu1, Jean-Valere Naubron2, Anamaria Hanganu1, Alexandru C Razus1, Simona Nica1.   

Abstract

A convenient enantioselective approach for the pinacol coupling of 1-acetylazulene involving easily accessible (R)- or (S)-BINOLs as chiral additive is reported. This supposes the preformation of the chiral titanium-BINOL complex in 1:2 ratio and subsequent reduction with zinc when, 2,3-di(azulen-1-yl)butane-2,3-diol can be isolated in around 60% enantiomeric excess. The absolute configuration of the isolated enantiomers was assigned by comparison of the experimental and Boltzmann-weighted calculated VCD and ECD spectra and assigned as (+)-(2S;3S)-di(azulen-1-yl)butane-2,3-diol. Chirality 27:826-834, 2015.
© 2015 Wiley Periodicals, Inc. © 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  2,3-di(azulen-1-yl)butane-2,3-diol; asymmetric pinacol coupling; catalytic reactions; circular dichroism spectroscopy; theoretical calculations

Year:  2015        PMID: 26364568     DOI: 10.1002/chir.22523

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Synthesis and properties of fluorescent 4'-azulenyl-functionalized 2,2':6',2″-terpyridines.

Authors:  Adrian E Ion; Liliana Cristian; Mariana Voicescu; Masroor Bangesh; Augustin M Madalan; Daniela Bala; Constantin Mihailciuc; Simona Nica
Journal:  Beilstein J Org Chem       Date:  2016-08-11       Impact factor: 2.883

  1 in total

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