Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315446
Title: Organic thionitroso compounds
Author: Taylor, Paul
ISNI:       0000 0001 2411 4502
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 1989
Availability of Full Text:
Access through EThOS:
Access through Institution:
Abstract:
A series of novel N-substituted phthalimide-2-sulplienamides was prepared. The N-aryl analogues were shown to be efficient precursors to thionitrosoarenes. Extension of the methodology to heteroaroraatic and acyl derivatives was unsuccessful, with the exception of 3-thionitroso- pyridine, the first known thionitrosoheteroarene. Thionitrosoarenes are shown to be versatile dienophiles and enophiles. Reactions with various substituted dienes proceeded with high stereoselectivity and some regioselectivity to afford 3,6-dihydro- 1,2-thiazines. Cycloadditions of thionitrosoarenes generated independently from imidosulphurous chloride precursors showed similar selectivities. The mechanism of cycloaddition is discussed in the light of molecular orbital calculations.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.315446  DOI: Not available
Keywords: Organic chemistry Chemistry, Organic
Share: