1. For examples of monofunctionalization of diols and diamines, see: (a) Reguillon, A.-F.; Dioury, F.-S.; Bouda, L.-N.; Cosma, C.; Siaugue, J.-M.; Foos, J.; Guy, A. Synlett 2000, 868; (b) McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388.
2. Cyclization catalyzed by palladium(0). Initial studies and macrolide formation
3. Facile routes to natural acyclic polyenes syntheses of spilanthol and trail pheromone for termite
4. For a comprehensive overview using the dithiocarbonyl functionality as an intermediate in organic syntheses, see: Dunn, A. D.; Rudorf, W.-D. In Carbon Disulphide in Organic Chemistry; Ellis Horwood Limited: England, 1989; pp. 226–367
5. For the synthetic use of dithiocarbonates in olefin preparation via the Chugaev reaction, see: Depuy, C. H.; King, R. W. Chem. Rev. 1960, 60, 432.