Ferrocene derivatives of liquid chiral molecules allow assignment of absolute configuration by X-ray crystallography

Tetrahedron Asymmetry

Volumn 28, Issue 10, 2017, Pages 1321-1329

  Holstein, Philipp M ^a   Holstein, Julian J ^b   Escudero Adán, Eduardo C ^a   Baudoin, Olivier ^c   Echavarren, Antonio M ^a,d  

^a BARCELONA INSTITUTE OF SCIENCE AND TECHNOLOGY   (Spain)

^b TU DORTMUND UNIVERSITY   (Germany)

^c UNIVERSITY OF BASEL   (Switzerland)

^d UNIVERSITAT ROVIRA I VIRGILI   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLESTANYL FERROCENE CARBOXYLATE; CHOLESTERYL FERROCENE CARBOXYLATE; EUGENYL FERROCENE CARBOXYLATE; FERROCENE DERIVATIVE; GERANYL FERROCENE CARBOXYLATE; N (1 HYDROXY 1 PHENYLPROPAN 2 YL) N FERROCENYL; N (HIOPHEN 2 YLMETHYL)FERROCENYL AMIDE; NERYL FERROCENE CARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CRYSTAL STRUCTURE; CRYSTALLIZATION; DERIVATIZATION; ELECTROSPRAY MASS SPECTROMETRY; MELTING POINT; NUCLEOPHILICITY; PRIORITY JOURNAL; SAPONIFICATION; STEREOCHEMISTRY; SUBSTITUTION REACTION; THERMOSTABILITY; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION;

EID: 85030767746     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2017.09.002     Document Type: Article

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