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Diels–Alder reactions of 1,1,4,4-tetrafluorobutatriene
Chemical Communications, 2010At 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
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Diels-Alder reaction, inverse electronic demand Diels-Alder reaction, hetero-Diels-Alder reaction
2002The 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.
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The Dehydro-Diels−Alder Reaction
Chemical Reviews, 2008Pablo, Wessig, Gunnar, Müller
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1995
Boron in Diels-Alder reactions falls into three categories: simple alkenylboranes as dienophiles, dienylboranes as dienes, and asymmetric boranes as acid catalysts that are chiral templates.
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Boron in Diels-Alder reactions falls into three categories: simple alkenylboranes as dienophiles, dienylboranes as dienes, and asymmetric boranes as acid catalysts that are chiral templates.
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The mechanism of the Diels-Alder reaction
Tetrahedron, 1959R.B. Woodward, Thomas J. Katz
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Diels-Alder Reactions of Trichlorophosphaethene
The Journal of Organic Chemistry, 1995Teunissen, H.T. +5 more
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Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
Angewandte Chemie - International Edition, 2020Russell Cox, Elizabeth Skellam
exaly
Catalytic Asymmetric Diels–Alder and Hetero-Diels–Alder Reactions
2003K. Mikami, Y. Matsumoto, T. Shiono
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