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- Q21856650 subject Q7400695.
- Q21856650 abstract "Cycloisomerization is any isomerization in which the cyclic isomer of the substrate is produced in the reaction coordinate. The greatest advantage of cycloisomerization reactions is its atom economical nature, by design nothing is wasted, as every atom in the starting material is present in the product. In most cases these reactions are mediated by a transition metal catalyst, in few cases organocatalysts and rarely do they occur under thermal conditions. These cyclizations are able to be performed with excellent levels of selectivity in numerous cases and have transformed cycloisomerization into a powerful tool for unique and complex molecular construction. Cyclosiomerization is a very broad topic in organic synthesis and many reactions that would be categorized as such exist. Two basic classes of these reactions are intramolecular Michael addition and Intramolecular Diels–Alder reactions. Under the umbrella of cycloisomerization, enyne and related olefin cycloisomerizations are the most widely used and studied reactions.".
- Q21856650 thumbnail Figure1cycloedit.png?width=300.
- Q21856650 wikiPageWikiLink Q127950.
- Q21856650 wikiPageWikiLink Q159226.
- Q21856650 wikiPageWikiLink Q192678.
- Q21856650 wikiPageWikiLink Q19588.
- Q21856650 wikiPageWikiLink Q201479.
- Q21856650 wikiPageWikiLink Q212270.
- Q21856650 wikiPageWikiLink Q2181524.
- Q21856650 wikiPageWikiLink Q2945392.
- Q21856650 wikiPageWikiLink Q375669.
- Q21856650 wikiPageWikiLink Q528995.
- Q21856650 wikiPageWikiLink Q59078.
- Q21856650 wikiPageWikiLink Q642233.
- Q21856650 wikiPageWikiLink Q66194.
- Q21856650 wikiPageWikiLink Q7400695.
- Q21856650 wikiPageWikiLink Q745930.
- Q21856650 wikiPageWikiLink Q898995.
- Q21856650 wikiPageWikiLink Q900337.
- Q21856650 wikiPageWikiLink Q903420.
- Q21856650 wikiPageWikiLink Q903758.
- Q21856650 wikiPageWikiLink Q904718.
- Q21856650 wikiPageWikiLink Q908086.
- Q21856650 comment "Cycloisomerization is any isomerization in which the cyclic isomer of the substrate is produced in the reaction coordinate. The greatest advantage of cycloisomerization reactions is its atom economical nature, by design nothing is wasted, as every atom in the starting material is present in the product. In most cases these reactions are mediated by a transition metal catalyst, in few cases organocatalysts and rarely do they occur under thermal conditions.".
- Q21856650 label "Cycloisomerization".
- Q21856650 depiction Figure1cycloedit.png.