Sugiyama, H.; Yokokawa, F.; Aoyama, T.; Shioiri, T. published the artcile< Synthetic studies of N-reverse prenylated indole. An efficient synthesis of antifungal indole alkaloids and N-reverse prenylated tryptophan>, Safety of (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is reverse prenylated indole preparation; antifungal alkaloid reverse prenylated tryptophan.
The efficient method for the synthesis of N-1,1-dimethyl-2-propenyl (reverse prenyl) indole was developed by the N-propargylation of the indoline, partial hydrogenation of the terminal alkyne, and oxidation to the indole using chem. manganese dioxide (CMD). This method was used for the synthesis of the antifungal indole alkaloids I, II, and N-reverse prenylated tryptophan.
Tetrahedron Letters published new progress about Fungicides. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Safety of (9Z,12Z)-Methyl octadeca-9,12-dienoate.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics