NERYLTRIETHYLAMMONIUM AND GERANYLTRIETHYLAMMONIUM HALIDES IN THE ALLYLATION OF SODIUM DIETHYL MALONATE - THE EFFECT OF THE LEAVING GROUP OFTHE ALLYLATING REAGENT ON THE SELECTIVITY OF THE REACTION

Citation
Ea. Petrushkina et Li. Zakharkin, NERYLTRIETHYLAMMONIUM AND GERANYLTRIETHYLAMMONIUM HALIDES IN THE ALLYLATION OF SODIUM DIETHYL MALONATE - THE EFFECT OF THE LEAVING GROUP OFTHE ALLYLATING REAGENT ON THE SELECTIVITY OF THE REACTION, Russian chemical bulletin, 43(2), 1994, pp. 249-251
Citations number
15
Categorie Soggetti
Chemistry
Journal title
ISSN journal
10665285
Volume
43
Issue
2
Year of publication
1994
Pages
249 - 251
Database
ISI
SICI code
1066-5285(1994)43:2<249:NAGHIT>2.0.ZU;2-D
Abstract
In the absence of catalysts, N-neryl- and N-geranyltriethylammonium ha lides can allylate sodium diethyl malonate to give terpene malonate de rivatives. Using the above-mentioned ammonium salts, geranyl and neryl acetates, geranyl ethyl carbonate, and geranyl diethyl phosphate as e xamples, it has been shown that with Pd-0 and Pd-II catalysts, the sel ectivity of the formation of neryl-, geranyl-, and linalylmalonates ca n be governed by varying the leaving group of the allylating agent.