Molecules 2000, 5(9), 1068-1079; doi:10.3390/50901068
Review

Recent Advances in the Substitution Reactions of Triorganylstannyl Ions with Aromatic Compounds by the SRN1 Mechanism. Synthetic Applications

Eduardo F. Córsico, Al Postigo and Roberto A. Rossi* email
INFIQC, Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba. Ciudad Universitaria, 5000 Córdoba, Argentina
* Author to whom correspondence should be addressed.
Received: 30 May 2000; in revised form: 18 August 2000 / Accepted: 5 September 2000 / Published: 11 September 2000
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Abstract: A review on the reactions of triorganyl stannyl ions with haloarenes is presented. Emphasis on the synthetic applications of the resulting triorganyl stannyl aryl compounds is made, with their inherent potential to build large molecules through the SRN1 sequence, i.e. ArX→ArSnR3→ArAr, which can be iteratively repeated when appropriately substituted substrates are chosen.
Keywords: stannyl anions; SRN1; Stille reactions

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MDPI and ACS Style

Córsico, E.F.; Postigo, A.; Rossi, R.A. Recent Advances in the Substitution Reactions of Triorganylstannyl Ions with Aromatic Compounds by the SRN1 Mechanism. Synthetic Applications. Molecules 2000, 5, 1068-1079.

AMA Style

Córsico EF, Postigo A, Rossi RA. Recent Advances in the Substitution Reactions of Triorganylstannyl Ions with Aromatic Compounds by the SRN1 Mechanism. Synthetic Applications. Molecules. 2000; 5(9):1068-1079.

Chicago/Turabian Style

Córsico, Eduardo F.; Postigo, Al; Rossi, Roberto A. 2000. "Recent Advances in the Substitution Reactions of Triorganylstannyl Ions with Aromatic Compounds by the SRN1 Mechanism. Synthetic Applications." Molecules 5, no. 9: 1068-1079.

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