Reaction of 6, 8-di-tert-butylspiro[4,5]deca-1-oxa-5,8-diene-2,7-dione with acid agents View Full Text


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Article Info

DATE

1982-07

AUTHORS

A. A. Volod'kin, R. D. Malysheva, V. V. Ershov

ABSTRACT

ConclusionsThe action of acid agents on 6, 8-di-tert-butylspiro[4.5]deca-1-oxa-5,8-diene-2,7-dione results in the initial opening of the lactone ring with a retention of the cyclohexadiene structure, and then the isomerization of the thus formed carbonium ion with migration of the carbonium ion center in two directions, and specifically in the six-membered ring and in the side chain.The migration direction of the intermediately formed carbonium ion depends on the temperature. More... »

PAGES

1454-1456

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00954174

DOI

http://dx.doi.org/10.1007/bf00954174

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1032408107


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