Conformational distortions from local symmetry in cyclic and acyclic compounds: Crystallographic data analysis of C3CZCC3 fragments (Z = C, P, Si, N, S, O).
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Description of molecular distortions in terms of symmetry coordinates
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3. Chemical reaction paths. 8. Stereoisomerization path for triphenylphosphine oxide and related molecules: indirect observation of the structure of the transition state
4. Chemical reaction paths. 9. Conformational interconversions of Wilkinson's catalyst and of related square-planar XM(PR3)3 compounds as determined from systematic analysis of solid-state structural data
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1. Bond angle distortion of C3CZCC3 fragments (Z = C, N, P, S, O, Si) by CZC opening and symmetrical C3C- distortion. Analysis of crystallographic data by perturbation of symmetry distortion coordinates.;Tetrahedron Letters;1987-01
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