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- W2039659898 endingPage "110" @default.
- W2039659898 startingPage "88" @default.
- W2039659898 abstract "The palladium-catalyzed arylation and alkenylation of alkenes, generally called the Heck reaction, has been applied to a number of new concepts. Starting from simple, oligohalogenated alkenes and arenes, the synthesis of a variety of highly functionalized carbon skeletons has been established. The domino-type combination of an intramolecular Heck with an inter- or intramolecular Diels–Alder reaction has been shown to provide facile access to interesting bicyclic and tetracyclic frameworks. While intramolecular Heck reactions on trisubstituted, cyclopropylidene-terminated alkenes proceeded with retention of the cyclopropyl moiety, tetrasubstituted alkenes with methylenecyclopropane end groups reacted with ring opening to yield cross-conjugated trienes. The study of the palladium-catalyzed oligocyclizations of 2-bromoalka-1,(ω-1)-diene-n-ynes has revealed interesting and useful systematics as to achievable ring size combinations and skeletal types. Highly functionalized methylenecyclopropanes are conveniently accessible via palladium-catalyzed allylic substitution reactions of 1-ethenylcyclopropyl sulfonates and chlorides as well as cyclopropylideneethyl esters which proceed with complete regioselectivity in most cases." @default.
- W2039659898 created "2016-06-24" @default.
- W2039659898 creator A5052144587 @default.
- W2039659898 creator A5056358838 @default.
- W2039659898 date "1999-03-01" @default.
- W2039659898 modified "2023-10-18" @default.
- W2039659898 title "Palladium in action: domino coupling and allylic substitution reactions for the efficient construction of complex organic molecules" @default.
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