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Updated: Jul 13, 2026

Solid Phase Synthesis of a Functionalized Bis-Peptide Using "Safety Catch" Methodology
11:42

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Published on: May 15, 2012

La diastereoselección acíclica en la adición radical proquiral a las olefinas proquiral

Mukund P Sibi1, Tara R Rheault, Sithamalli V Chandramouli

  • 1Department of Chemistry, North Dakota State University, Fargo, ND 58105-5516, USA. Mukund.Sibi@ndsu.nodak.edu

Journal of the American Chemical Society
|March 21, 2002
PubMed
Resumen

Comprender las preferencias estereoquímicas en las reacciones radicales es clave. Este estudio encontró que los efectos estereoelectrónicos, no solo la masa estérica, son cruciales para la alta selectividad en las adiciones de radicales procirales.

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