Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Donald K. Cameron"'
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ChemInform Abstract: Application of 3-Oxabicyclo(3.2.0)hept-6-ene-2,4-dione (Cyclobut-3-ene- 1,2-dicarboxylic Anhydride) as an Acetylene Equivalent in Cycloadditions
Autor: Stuart J. Wyse, J. I. G. Cadogan, Donald K. Cameron, Ian Gosney, Edward J. Tinley, Alicia Amaro
Publikováno v: ChemInform. 22
The effectiveness and limitations of dioxo-3-oxabicyclo[3.2.0]hept-6-ene-2,4-dione (cyclobut-3ene-1,2-dicarboxylic anhydride) as an acetylene equivalent in both 1,3-dipolar and Diels–Alder cycloadditions is reported; it reacted readily with a varie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0d060e4da330c67f51a511f60e41de3e
https://doi.org/10.1002/chin.199149071
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2
Intramolecular nucleophilic interception by the sulfonyl group of reaction intermediates arising from electrophilic addition to unsaturated non-conjugated bicyclic sulfones
Autor: J. I. G. Cadogan, Donald K. Cameron, John R. A. Millar, Stephen F. Newlands, Ian Gosney, David W. Reed
Publikováno v: Journal of the Chemical Society, Perkin Transactions 2. :2309
Electrophilic addition of molecular bromine and related reactions to unsaturated bicyclic sulfones resulting in atypical addition is described. Bromination of the bicyclic sulfone 3 results in a ca. 1 : 1 mixture of exo,exo- and exo,endo-dibromides 4
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::589a23f10d8cc4340dc710fdd2d5991a
https://doi.org/10.1039/p29960002309
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3
Application of 3-oxabicyclo[3.2.0]hept-6-ene-2,4-dione (cyclobut-3-ene-1,2-dicarboxylic anhydride) as an acetylene equivalent in cycloadditions
Autor: J. I. G. Cadogan, Alicia Amaro, Donald K. Cameron, Stuart J. Wyse, Ian Gosney, Edward J. Tinley
Publikováno v: Journal of the Chemical Society, Perkin Transactions 1. :2081
The effectiveness and limitations of dioxo-3-oxabicyclo[3.2.0]hept-6-ene-2,4-dione (cyclobut-3ene-1,2-dicarboxylic anhydride) as an acetylene equivalent in both 1,3-dipolar and Diels–Alder cycloadditions is reported; it reacted readily with a varie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aec58897ad650bc9f09dc9336048627f
https://doi.org/10.1039/p19910002081
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6
The sulphone group as a nucleophile: intramolecular formation of a novel thiadecanylium tribromide via addition of bromine to a double bond in an overcrowded environment
Autor: Stephen F. Newlands, Donald K. Cameron, Rona M. Highcock, Ian Gosney, J. I. G. Cadogan
Publikováno v: Journal of the Chemical Society, Chemical Communications. :766
Instead of furnishing a normal bromide addition product, bromination of 4-thiatricyclo[5.2.0.02,6]non-8-ene 4-4-dioxide (1) gives 5-bromo-1-oxo-10-oxa-1λ6-thiatetracyclo[4.3.1.03,8.04,7]decan-1-ylium tribromide (3) through intramolecular reaction of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::50aec34333376664614508ef8896b810
https://doi.org/10.1039/c39860000766
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7
Divergent thermal behaviour of phenoxymethyl phenyl sulphoxide under gas and condensed-phase conditions
Autor: Angus R. Brown, Donald K. Cameron, J. I. G. Cadogan, Ian Gosney, Malcolm R. Banks
Publikováno v: Journal of the Chemical Society, Perkin Transactions 2. :595
A comparison is made between the behaviour of phenoxymethyl phenyl sulphoxide (2) under different thermolytic conditions. Passage of (2) through a quartz tube in the gas phase at 600 °C results in products which can be rationalised by assuming homol
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2dcfa006a1852936a88c94553a6d7b8c
https://doi.org/10.1039/p29890000595
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