Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Stuart J. Wyse"'
Autor:
Stuart J. Wyse, Ian Gosney, Leo M. McLaughlin, R. Alan Aitken, J. I. G. Cadogan, Caroline M. HumphrieséBuchan
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :605-614
Functionalisation of the double bond of 3-thiabicyclo[3.2.0]hept-6-ene 3, readily formed by hydrolysis of the [2+2] cycloadduct 1 of 3-sulfolene and maleic anhydride followed by oxidative bis-decarboxylation, gives tricyclic sulfones 5–7 and 9 with
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
Autor:
J. I. G. Cadogan, Stuart J. Wyse, Ian Gosney, Caroline M. Humphries, R. Alan Aitken, Leo M. McLaughlin
Publikováno v:
ChemInform. 30
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