Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 20880-92-6, Name is ((3aS,5aR,8aR,8bS)-2,2,7,7-Tetramethyltetrahydro-3aH-bis([1,3]dioxolo)[4,5-b:4′,5′-d]pyran-3a-yl)methanol, SMILES is OC[C@@]1([C@H]([C@@H]([C@@H](CO1)O2)OC2(C)C)O3)OC3(C)C, in an article , author is Egorova, AY, once mentioned of 20880-92-6, Category: pyrrolines.
Synthesis of arylidene derivatives of N-unsubstituted pyrrolin-2-ones
5-Alkyl(aryl)-3-arylidene-3H-pyrrolin-2-ones were synthesized by ammonolysis of their O-heteroanalogs or by the reactions of 5-alkyl(aryl)-3H-pyrrolin-2-ones with aromatic aldehydes. The structures of the compounds obtained were confirmed by H-1 NMR spectra.
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Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem