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The synthesis and reactivity of a sterically unhindered phosphanylidene-phosphorane & the reduction of 1,3,2,4-dithiadiphosphetane-2,4-disulfides to primary and tertiary phosphines
Item metadata
dc.contributor.advisor | Kilian, Petr | |
dc.contributor.advisor | Woollins, J. D. (J. Derek) | |
dc.contributor.author | Surgenor, Brian A. | |
dc.coverage.spatial | xvii, 314 p. | en_US |
dc.date.accessioned | 2013-11-12T15:56:11Z | |
dc.date.available | 2013-11-12T15:56:11Z | |
dc.date.issued | 2013-07-24 | |
dc.identifier | uk.bl.ethos.581849 | |
dc.identifier.uri | https://hdl.handle.net/10023/4187 | |
dc.language.iso | en | en_US |
dc.publisher | University of St Andrews | |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ | |
dc.subject | Tertiary phosphines | en_US |
dc.subject | Low coordinate phosphorus | en_US |
dc.subject | Phosphanylidene-phosphorane | en_US |
dc.subject | Ferrocene | en_US |
dc.subject | Phosphinidene | en_US |
dc.subject | Primary phosphines | en_US |
dc.subject | Dichloro phosphines | en_US |
dc.subject | Preparative scale development | en_US |
dc.subject.lcc | QD406.S8 | |
dc.subject.lcsh | Organophosphorus compounds | en_US |
dc.subject.lcsh | Organophosphorus compounds--Synthesis | en_US |
dc.title | The synthesis and reactivity of a sterically unhindered phosphanylidene-phosphorane & the reduction of 1,3,2,4-dithiadiphosphetane-2,4-disulfides to primary and tertiary phosphines | en_US |
dc.type | Thesis | en_US |
dc.type.qualificationlevel | Doctoral | en_US |
dc.type.qualificationname | PhD Doctor of Philosophy | en_US |
dc.publisher.institution | The University of St Andrews | en_US |
dc.rights.embargodate | 2021-10-10 | en_US |
dc.rights.embargoreason | Thesis restricted in accordance with University regulations. Print and electronic copy restricted until 10th October 2021 | en_US |
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