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dc.contributor.authorMartınez Isamir.
dc.contributor.authorAndrews Alexander E.
dc.contributor.authorEmch Joseph D.
dc.contributor.authorNdakala Albert J.
dc.contributor.authorWang Jun.
dc.contributor.authorHowell Amy R.
dc.date.accessioned2013-03-27T11:07:17Z
dc.date.issued2003
dc.identifier.citationOrganic letters. 2003 feb20; Vol.5,No.4. 399-402en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/15189
dc.description.abstract[reaction: see text] 3-Alkylidene-2-methyleneoxetanes have been prepared by treating alpha-alkylidene-beta-lactones, derived from Morita-Baylis-Hillman-type adducts, with dimethyltitanocene. Preliminary studies of the reactivity of these little known, strained heterocycles are also described.en
dc.language.isoenen
dc.publisher© 2003 American Chemical Societyen
dc.subjectUnusualen
dc.subjectStrained Heterocyclesen
dc.subject3-Alkylidene-2-methyleneoxetanesen
dc.subjectMorita-Baylis-Hillman-type Adductsen
dc.titleUnusual, Strained Heterocycles: 3-Alkylidene-2-methyleneoxetanes from Morita-Baylis-Hillman-type Adductsen
dc.typeArticleen
local.publisherSchool of Physical Sciencesen


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