Regioselective bond cleavage and coordination effects in the reduction of some acetals with lithium in ammonia

Simple item page
dc.contributor.authorAbell, A.D.
dc.contributor.authorMassywestropp, R.A.
dc.date.issued1985
dc.description.abstractSome benzylic-type acetals possessing the 2,8-dioxa-bicyclo [3.2.1]octane ring system are cleaved in a regioselective manner when treated with lithium in ammonia. The results from various reductions implicate coordination of lithium as a significant factor involved in reduction mechanisms.
dc.description.statementofresponsibilityA.D. Abell and R.A. Massy-Westropp
dc.identifier.citationTetrahedron: the international journal for the rapid publication of full original research papers and critical reviews in organic chemistr, 1985; 41(12):2451-2464
dc.identifier.doi10.1016/S0040-4020(01)96640-2
dc.identifier.issn0040-4020
dc.identifier.issn1464-5416
dc.identifier.orcidAbell, A.D. [0000-0002-0604-2629]
dc.identifier.urihttp://hdl.handle.net/2440/86623
dc.language.isoen
dc.publisherPergamon Press
dc.rightsCopyright © 1985
dc.source.urihttps://doi.org/10.1016/s0040-4020(01)96640-2
dc.titleRegioselective bond cleavage and coordination effects in the reduction of some acetals with lithium in ammonia
dc.typeJournal article
pubs.publication-statusPublished

Files

Collections

Chemistry publications