Kelly, T. Ross; Ohashi, Naohito; Armstrong-Chong, Rosemary J.; Bell, Stephen H. published the artcile< Synthesis of (±)-fredericamycin A>, Name: 2,2-Diethoxyacetonitrile, the main research area is fredericamycin A.
(±)-Fredericamycin A (I) was prepared via the regiospecific, Me3Si-directed coupling of indane II with anhydride III to give the coupling product IV. Formation of the spiro system is achieved by reduction of IV to a keto aldehyde which undergoes in situ cyclization to the spiro ketols.
Journal of the American Chemical Society published new progress about 6136-93-2. 6136-93-2 belongs to class nitriles-buliding-blocks, and the molecular formula is C6H11NO2, Name: 2,2-Diethoxyacetonitrile.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts