Keywords: Dendrimers / Fragrances / Neighboring-group effects / Kinetics / Delivery systems / Controlled release 2-Carbamoylbenzoates which are chemically bound to the surface of dendrimers were found to release tertiary fragrance alcohols by neighbouring group assisted alkaline hydrolysis under mild reaction conditions. Owing to the excellent separation of the intermediate reaction products by analytical HPLC, the kinetic rate constants of the first two consecutive reaction steps of fragrance release could be
A new route to an H 1 -H 3 antagonist was developed to address scalability and environmental and cost of goods issues associated with the initial route.
Regioselective isomerisation of epoxides to allylic alcohols can be achieved using p-toluenesulfonic acid in the presence of 1,3-dimethylimidazolidin-2-one.The regioselective isomerisation of an unsymmetrically substituted epoxide into an allylic alcohol is a very valuable transformation for organic synthesis. 1 The Sharpless protocol 2 of ring opening with phenylselenide anion followed by hydrogen peroxide induced syn elimination of the resultant selenoxide is now a recognised method for introduction of the double bond at the less hindered terminus. For alkene formation at the more hindered site, the use of a stoichiometric amount of a strong chelating base possessing an oxophilic metal cation, such as lithium diethylamide or diethylaluminium 2,2,6,6-tetramethylpiperidide, has often proven to be the method of choice. 3 By way of contrast, efforts to control the evolution of an incipient carbocation intermediate generated by coordination of a Brønsted or Lewis acid to the oxygen lone pair can be fraught with danger, inasmuch as several competing pathways including hydride shift, alkyl shift, proton loss, and nucleophilic capture can all compete. 4 This situation is summarised in Scheme 1 for the simple case of 1-methylcyclohexene oxide and clearly indicates that careful selection of both cation and counterion is required to direct a desired pathway.In terms of allylic alcohol formation, our own studies were therefore inspired by a method developed by Noyori 5 involving sequential ring opening with trimethylsilyl triflate in the presence of 2,6-lutidine followed by anti elimination from the unstable diequatorial triflate using DBU (Scheme 1). The results of a simple preliminary experiment in which efforts were made to replace the silicon electrophile by a proton from p-toluenesulfonic acid and the nucleophile by DMF in order to create a positively charged leaving group were completely unsuccessful and merely served to illustrate the aforementioned complexity of the situation (Scheme 2).
Scheme 1Scheme 2
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.