Literature DB >> 23282912

Enantiomerically pure and racemic dimethyl{N-[(2-oxidonaphthalen-1-yl-κO)methylidene]valinato-κ2N,O}tin(IV).

Uwe Böhme1, Sabine Fels.   

Abstract

The title compound, [Sn(CH(3))(2)(C(16)H(15)NO(3))], crystallized from one reaction batch with high enantiomeric excess as both a pure enantiomer and a racemate. The S enantiomer crystallizes in the chiral space group P3(2). The racemate crystallizes in the space group P1 with R and S enantiomers in the crystal lattice; these form dimers about a crystallographic inversion centre.

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Year:  2012        PMID: 23282912     DOI: 10.1107/S0108270112050470

Source DB:  PubMed          Journal:  Acta Crystallogr C        ISSN: 0108-2701            Impact factor:   1.172


  1 in total

1.  Absolute structure of the chiral pyrrolidine derivative (2S)-methyl (Z)-5-(2-tert-butoxy-1-cyano-2-oxoethylidene)pyrrolidine-2-carboxylate, a compound with low resonant scattering.

Authors:  Ai Wang; Ulli Englert
Journal:  Acta Crystallogr C Struct Chem       Date:  2019-10-04       Impact factor: 1.172

  1 in total

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