When cobalt-mediated [2+2+2] cycloaddition reaction dares go astray: synthesis of unprecedented cobalt(iii)-complexes

被引：4
|
作者：
Delorme, Marion [1 ]
Punter, Alexander [1 ]
Oliveira, Raquel [2 ]
Aubert, Corinne [3 ]
Carissan, Yannick [1 ]
Parrain, Jean-Luc [1 ]
Amatore, Muriel [1 ]
Nava, Paola [1 ]
Commeiras, Laurent [1 ]
机构：
[1] Aix Marseille Univ, CNRS, Cent Marseille, iSm2, Marseille, France
[2] Sorbonne Univ, PSL Univ, CNRS, Ecole Normale Super,PASTEUR,Dept Chim, F-75005 Paris, France
[3] Sorbonne Univ, Inst Parisien Chim Mol, UPMC, Univ Paris 06,UMR 8232,CNRS, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
来源：
DALTON TRANSACTIONS | 2019年 / 48卷 / 42期
关键词：
TRANSITION-METALS; H ACTIVATION; BASIS-SETS; C-H; ALKYNES; CYCLOTRIMERIZATION; COBALTACYCLOPENTADIENE; COOLIGOMERIZATION; APPROXIMATION; COMPLEXES;
D O I：
10.1039/c9dt03311d
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
In sharp contrast with the standard [2 + 2 + 2] cycloaddition reaction of diyne/ene, cobalt-mediated cycloadditions with gamma-alkylidenebutenolide led to unprecedented cobalt(iii) polycyclic complexes. A plausible mechanism supported by a computational study based on an unusual fragmentation of the butenolide moiety was postulated to account for this original reaction.
引用
收藏
页码：15767 / 15771
页数：5
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