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Morita–Baylis–Hillman adduct derivatives (MBHADs): versatile reactivity in Lewis base-promoted annulation
Organic & Biomolecular Chemistry · 2015 · Vol. 13(32) · pp. 8578–8595
Peizhong Xie(Collaborative Innovation Center of Chemical Science and Engineering Tianjin)You Huang✉(Collaborative Innovation Center of Chemical Science and Engineering Tianjin)
Abstract
Lewis base-promoted annulation reactions with MBHADs have emerged as a key platform for the construction of functionalized carbo- and heterocycles. MBHADs, which are economical and readily available, exert diverse and amazing reactivity when reacted with a wide range of electrophiles. A variety of carbo- and heterocycles, most of which are predominant in natural products and pharmaceuticals, could be constructed with high efficiency. This tutorial review will describe these annulation reactions, with a special emphasis on recent work regarding diverse reactivities of MBHADs.
Asymmetric Synthesis and CatalysisCatalytic C–H Functionalization MethodsChemical Synthesis and ReactionsAnnulationChemistryLewis acids and basesElectrophileAdductReactivity (psychology)Combinatorial chemistryOrganic chemistryCatalysis
MeSH terms
AlcoholsCyclizationPolycyclic CompoundsMolecular StructureLewis Bases
Funding
- National Natural Science Foundation of China
- Specialized Research Fund for the Doctoral Program of Higher Education of China
Citations
308
FWCI
20.04
field-weighted impact
References
54
Percentile
100%
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Citations per year
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