Reduction of Carboxamides Into Amines Catalyzed by La[NH‐2,6‐iPr2‐4‐FcC6H2]3/HBpin

Fuente: Wiley Open Access
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Qiujin Ye, Yukun Wang, Jue Chen, Yunjie Luo
Format: Artículo Open Access
Veröffentlicht: Wiley 2024
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1867013924032872449
author Qiujin Ye
Yukun Wang
Jue Chen
Yunjie Luo
author_facet Qiujin Ye
Yukun Wang
Jue Chen
Yunjie Luo
Qiujin Ye
Yukun Wang
Jue Chen
Yunjie Luo
collection Wiley Open Access
contents Reduction of Carboxamides Into Amines Catalyzed by La[NH‐2,6‐iPr2‐4‐FcC6H2]3/HBpin Qiujin Ye Yukun Wang Jue Chen Yunjie Luo Applied Organometallic Chemistry ABSTRACTReduction of carboxamides is an efficient approach to obtain the corresponding amines, albeit it is one of the most problematic. In this work, by use of pinacolborane (HBpin) as a reductant, the rare‐earth metal tris (arylamido) complex supported by a ferrocenyl‐modified arylamido ligand La[NH‐2,6‐iPr2‐4‐FcC6H2]3 was employed as a precatalyst for primary and secondary amide reductions. This catalyst system exhibited high activity toward hydroborative reduction of amides to amines under mild conditions, as well good tolerance for heteroatoms and functional groups in the reduction. A lanthanide hydride was experimentally verified as the active species and the reduction mechanism was proposed. 10.1002/aoc.7739 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/aoc.7739
format Artículo Open Access
id wiley_oa_10_1002_aoc_7739
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Reduction of Carboxamides Into Amines Catalyzed by La[NH‐2,6‐iPr2‐4‐FcC6H2]3/HBpin
Qiujin Ye
Yukun Wang
Jue Chen
Yunjie Luo
Applied Organometallic Chemistry
Reduction of Carboxamides Into Amines Catalyzed by La[NH‐2,6‐iPr2‐4‐FcC6H2]3/HBpin Qiujin Ye Yukun Wang Jue Chen Yunjie Luo Applied Organometallic Chemistry ABSTRACTReduction of carboxamides is an efficient approach to obtain the corresponding amines, albeit it is one of the most problematic. In this work, by use of pinacolborane (HBpin) as a reductant, the rare‐earth metal tris (arylamido) complex supported by a ferrocenyl‐modified arylamido ligand La[NH‐2,6‐iPr2‐4‐FcC6H2]3 was employed as a precatalyst for primary and secondary amide reductions. This catalyst system exhibited high activity toward hydroborative reduction of amides to amines under mild conditions, as well good tolerance for heteroatoms and functional groups in the reduction. A lanthanide hydride was experimentally verified as the active species and the reduction mechanism was proposed. 10.1002/aoc.7739 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Reduction of Carboxamides Into Amines Catalyzed by La[NH‐2,6‐iPr2‐4‐FcC6H2]3/HBpin
topic Applied Organometallic Chemistry
url https://onlinelibrary.wiley.com/doi/10.1002/aoc.7739