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- Q6058463 subject Q7458901.
- Q6058463 subject Q9006606.
- Q6058463 abstract "In organic chemistry, an intramolecular Diels-Alder cycloaddition is a Diels–Alder reaction in which the diene and a dienophile are both part of the same molecule. The reaction leads to the formation of the same cyclohexene-like structure as usual for a Diels–Alder reaction, but as part of a more complex fused or bridged cyclic ring system.".
- Q6058463 thumbnail Corey_1978_gibberellic_acid.png?width=300.
- Q6058463 wikiPageWikiLink Q11081.
- Q6058463 wikiPageWikiLink Q1128023.
- Q6058463 wikiPageWikiLink Q157017.
- Q6058463 wikiPageWikiLink Q192678.
- Q6058463 wikiPageWikiLink Q206286.
- Q6058463 wikiPageWikiLink Q2715597.
- Q6058463 wikiPageWikiLink Q320584.
- Q6058463 wikiPageWikiLink Q375669.
- Q6058463 wikiPageWikiLink Q413328.
- Q6058463 wikiPageWikiLink Q413512.
- Q6058463 wikiPageWikiLink Q7458901.
- Q6058463 wikiPageWikiLink Q9006606.
- Q6058463 wikiPageWikiLink Q903429.
- Q6058463 comment "In organic chemistry, an intramolecular Diels-Alder cycloaddition is a Diels–Alder reaction in which the diene and a dienophile are both part of the same molecule. The reaction leads to the formation of the same cyclohexene-like structure as usual for a Diels–Alder reaction, but as part of a more complex fused or bridged cyclic ring system.".
- Q6058463 label "Intramolecular Diels–Alder cycloaddition".
- Q6058463 depiction Corey_1978_gibberellic_acid.png.
