A novel and convenient approach, the domino retro Diels-Alder/Diels-Alder reaction sequence for highly stereo- and regioselective synthesis of various bicyclo[2.2.2]octenone and bicyclo[2.2.2]octadienone derivatives is presented. Thus, the masked o-benzoquinones (MOBs) 2a-e generated by the pyrolysis of the respective dimers 3a-e participated in this novel synthetic strategy with a variety of o...

The Diels-Alder cycloadditions of cyclopentadiene and 2,3-dimethyl-1,3-butadiene to a range of 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions is described. The influence of reaction conditions on the outcome of the cycloadditions, in particular the stereoselectivity and reaction efficiency, is discussed. While the cycloadditions have been attempted at the sulfide, ...

A novel route to highly aromatic polyimides is presented and used form multiblock copolymers which inherently difficult achieve via traditional routes for this important polymer family.

Studies toward the enantiospecific total synthesis of rhodexin A via a very hindered inverse electron demand Diels-Alder reaction are described. The C8-diastereomer of the fully elaborated tetracyclic core of rhodexin A, 23, was prepared in good yield and excellent selectivity using as the key step the stepwise Diels-Alder reaction of the very hindered dienone 3 and the silyl enol ether 4 catal...

Two catalysts, Me(2)AlNTf(2) and MeAl(NTf(2))(2), derived from the mixing of trimethylaluminum with triflimide, proved to be highly effective catalysts in hindered Diels-Alder reactions, generating the desired Diels-Alder cycloadducts from both hindered 2-silyloxydienes and hindered dienophiles. Thus reaction of 1 with 2 afforded the hindered cycloadduct 4 in excellent yield in 0.5-1.5 h at -40...

The Carboni-Lindsey reaction between tetrazines and strained unsaturated hydrocarbons has in recent years become a useful tool bioorthogonal chemistry for labelling biomolecules vitro vivo. Here, we report computational studies on the mechanism of Diels-Alder/Retro-Diels-Alder commercially available tetrazine norbornene. Isomerism with norbornene-amide relevant applications bioconjugation chemi...

ABSTRACT Knoevenagel condensation of barbituric acids with aromatic aldehydes containing one or two formyl groups was carried out. 5-Arylidenebarbituric acids underwent smooth hetero-Diels-Alder (HDA) reactions with enol ethers to afford cis and trans diastereoisomers of pyrano[2,3-d]pyrimidine-2,4-diones and 5,5'-(1,4-phenylene)bis[2H-pyrano[2,3-d]pyrimidine-2,4(3H)-dione] derivatives in excel...

• Current review on Self-healing polymers based Diels-Alder cycloaddition. Discussing healing thermodynamics for physical and chemical changes during healing. Deeper insight use of advanced analytical/spectroscopic/modelling techniques. Use multifunctional mechanisms engineering applications. Future scope DA better commerciality green chemistry. The ability artificial materials to be healed eff...