In organic chemistry, the Diels–Alder reaction is a chemical reaction between a conjugated diene and a substituted alkene, commonly termed the dienophile...
62 KB (7,087 words) - 07:54, 21 July 2024
In organic chemistry, the hexadehydro-Diels–Alder (HDDA) reaction is an organic chemical reaction between a diyne (2 alkyne functional groups arranged...
19 KB (2,205 words) - 12:36, 6 August 2024
Cycloaddition (redirect from Cycloaddition reaction)
inverse electron-demand Diels–Alder reaction, Hexadehydro Diels-Alder reaction and the related alkyne trimerisation. The reaction can also be run in reverse...
11 KB (1,261 words) - 17:18, 22 January 2024
Aryne (section Reactions of arynes)
induces elimination of triflate and release of benzyne: A hexadehydro Diels-Alder reaction (HDDA) involves cycloaddition of 1,3-diyne and alkyne. N-amination...
28 KB (3,128 words) - 23:01, 27 July 2024
Alkyne trimerisation (category Carbon-carbon bond forming reactions)
example of a hexadehydro Diels–Alder reaction. Trimerisation of three 2-butyne (dimethylacetylene) molecules yields hexamethylbenzene. The reaction is catalyzed...
18 KB (1,925 words) - 02:15, 18 April 2024
refer to: D-glycero-alpha-D-manno-heptose-7-phosphate kinase Hexadehydro Diels-Alder reaction This disambiguation page lists articles associated with the...
135 bytes (48 words) - 17:47, 28 December 2019