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Azoliums and Ag(I)-N-Heterocyclic Carbene Thioglycosides: Synthesis, Reactivity and Bioactivity
被引:7
|作者:
Ryzhakov, Dmytro
[1
]
Beillard, Audrey
[2
]
Le Bideau, Franck
[1
]
Al-Shuaeeb, Riyadh Ahmed Atto
[1
]
Alami, Mouad
[1
]
Bantreilejoc, Xavier
[2
,3
]
Bonnemoy, Aurore
[4
]
Gautier, Arnaud
[4
]
Lamaty, Frederic
[2
]
Messaoudi, Samir
[1
]
机构:
[1] Univ Paris Saclay, BioCIS, CNRS, F-92290 Chatenay Malabry, France
[2] Univ Montpellier, ENSCM, CNRS, IBMM, Montpellier, France
[3] Inst Univ France IUF, Montpellier, France
[4] Univ Clermont Auvergne, ICCF, UMR 6296, CNRS, F-63000 Clermont Ferrand, France
关键词:
Glycosides;
Mechanochemistry;
Migita crosscoupling;
N-Heterocyclic carbenes;
Palladium;
N-HETEROCYCLIC CARBENES;
METAL-COMPLEXES;
SILVER(I)-CARBENE COMPLEXES;
ANTICANCER ACTIVITY;
CATALYTIC-ACTIVITY;
NHC LIGANDS;
CARBOHYDRATE;
EFFICIENT;
MECHANOCHEMISTRY;
COORDINATION;
D O I:
10.1002/ejoc.202101499
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A versatile protocol for the synthesis of azolium thioglycosides is reported. This protocol is based on a PdG3-catalyzed Migita cross-coupling between p-di-iodo azoliums and protected or unprotected beta-1-thioglucose partners. Moreover, a solvent-free mechanochemistry approach was developed as a unique access to the corresponding Ag(I)-N-heterocyclic carbene thioglycosides. Finally, chemical reactivity and antiproliferative bioactivity were examined with azoliums and Ag(I)-NHC thioglycosides. This study demonstrates a promising potential of these newly synthesized carbohydrate-based N-heterocyclic derivatives.
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页数:8
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