Results 221 to 230 of about 2,240,218 (271)

Three-component diels-alder reaction through palladium carbene migratory insertion enabled dearomative C(sp³)-H bond activation. [PDF]

Nat Commun
Mi Y, Liu S, Hu L, Wang Y, Luo R, Yu Y, Zhang Z, Yuan S, Lu G, Huang X.   +9 more
europepmc   +1 more source

Sustainable tandem acylation/Diels-Alder reaction toward versatile tricyclic epoxyisoindole-7-carboxylic acids in renewable green solvents. [PDF]

Beilstein J Org Chem
Yıldırım A.
europepmc   +1 more source

Kinetic Study of the Diels-Alder Reaction between Maleimide and Furan-Containing Polystyrene Using Infrared Spectroscopy. [PDF]

Polymers (Basel)
Wang T, Gao D, Yin H, Zhao J, Wang X, Niu H.   +5 more
europepmc   +1 more source

Inverse Electron Demand Diels-Alder Reaction on M₃N@C₈₀ (M=Lu, Sc): Reactivity and Reversibility Enable Chemical Separation of Metallofullerenes. [PDF]

Angew Chem Int Ed Engl
Sun Y, Abella L, Emge TJ, Zhu S, Li Y, Ferraro I, Li A, Stevenson S, Poblet JM, Rodríguez-Fortea A, Zhang J.   +10 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

The Dehydro-Diels−Alder Reaction

Chemical Reviews, 2008
Pablo Wessig
exaly   +3 more sources

Dehydrogenative Diels–Alder Reaction

Organic Letters, 2011
The dehydrogenative cycloaddition of dieneynes, which possess a diene in the form of a styrene moiety and a dienophile in the form of an alkyne moiety, produces naphthalene derivatives when heated. It was found that a key requirement of this process is the presence of a silyl group attached to the alkyne moiety, which forces a dehydrogenation reaction ...
Takuya, Ozawa, Takuya, Kurahashi, Seijiro, Matsubara   +2 more
openaire   +2 more sources

Oxazole Diels—Alder Reactions

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Jeremy I. Levin, Leif M. Laakso
openaire   +1 more source

Diels–Alder reactions of 1,1,4,4-tetrafluorobutatriene

Chemical Communications, 2010
At low temperature 1,1,4,4-tetrafluorobutatriene undergoes Diels-Alder reaction with various dienes; the structure of one product and its isomerisation derivative has been elucidated by X-ray crystallography.
Ehm, Christian, Lentz, Dieter
openaire   +3 more sources

Diels–Alder Reaction

2009
The Diels–Alder reaction, inverse electronic demand Diels–Alder reaction, as well as the hetero-Diels–Alder reaction, belong to the category of [4+2]-cycloaddition reactions, which are concerted processes.
openaire   +1 more source

Diels-Alder reaction, inverse electronic demand Diels-Alder reaction, hetero-Diels-Alder reaction

2002
The Diels-Alder reaction, reverse electronic demand Diels-Alder reaction, as well as the hetero-Diels-Alder reactions, belong to the category of [4+2] -cycloaddition reactions, which is a concerted process. The arrow-pushing here is merely illustrative.
openaire   +1 more source