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Updated: Jun 29, 2026

Hydrolysis of a Ni-Schiff-Base Complex Using Conditions Suitable for Retention of Acid-labile Protecting Groups
06:44

Hydrolysis of a Ni-Schiff-Base Complex Using Conditions Suitable for Retention of Acid-labile Protecting Groups

Published on: April 6, 2017

Reacción de Mannich enantioselectiva altamente diastereoselectiva y conmutable de los derivados de la glicina con las

Xiao-Xia Yan1, Qian Peng, Qing Li

  • 1State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China.

Journal of the American Chemical Society
|October 10, 2008
PubMed
Resumen

Los investigadores ajustaron la diastereoselectividad en las reacciones de Mannich utilizando nuevos catalizadores de cobre. Este método produce de manera eficiente derivados de ácido anti-o sin-alfa,beta-diamino con un alto control estereoquímico.

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