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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/3748

Title: Chelate ring size effect on the reactivity of [2-(2-phenyl-5,6-dihydro-4H-1,3-oxazinyl)]lithium and Se center dot center dot center dot N interactions in low-valent organoselenium compounds: Facile isolation of diorganotriselenide
Authors: KUMAR, S
KANDASAMY, K
SINGH, HB
WOLMERSHAUSER, G
BUTCHER, RJ
Keywords: glutathione-peroxidase activity
improved catalytic-activity
thiol peroxidase
antioxidant activity
hydrogen-peroxide
structural-characterization
diorganyl tellurides
remarkable activity
organochalcogen se
selenenic acid
Issue Date: 2004
Publisher: AMER CHEMICAL SOC
Citation: ORGANOMETALLICS, 23(18), 4199-4208
Abstract: The reaction of [2-(2-phenyl-5,6-dihydro-4H-1,3-oxazinyl)]lithium (13), containing a six-membered oxazine ring, with elemental selenium gave lithium aryldiselenolate (14) as the major reaction intermediate along with other polyselenolates (15 and 16), whereas [2-(4,4-dimethyl-2-phenyloxazolinyl]lithium (21), containing a five-membered oxazoline ring, on reaction with selenium gave only lithium arlyselenolate 22 under similar conditions. The unusual selenation reaction of aryllithium 13 has been studied by ES-MS spectrometry. The oxidative workup of in situ-generated lithium arylpolyselenolates (14-16) afforded a mixture of diorganopolyselenides (10, 11, 17, and 18), from which diorganotriselenide 11 was obtained as the major product, whereas lithium arylselenolate 22 gave only diselenide 6 on oxidation. Equimolar reactions of diorganotriselenide 11 with sulfuryl chloride and benzenethiol give the novel selenium halide [RSeSeCl (24)] and seleniumselenenyl sulfide (28), respectively. However, the reaction of triselenide 11 with an excess amount of halogenating reagents afforded selenenyl halides [RSeX; X = Cl (25), Br (26), 1 (27)]. The reaction of lithium arylpolyselenolates (14-16) with benzyl chloride gave a mixture of diselenide (10), unsymmetrical diselenide (31), benzyl selenide (32), and dibenzyl diselenide (33). The reaction of 14-16 with a.,W-dibromo-ortho-xylene gave the 10-membered diselenocine (34) and 26. GPx-like activities of diselenide 10 and triselenide 11 have been evaluated by using both benzenethiol and coupled reductase assay methods. Triselenide 11 shows much better GPx-like activity than diselenide 10. Crystal structures of organoselenium compounds (11, 25-27, 29, 32, and 34) were determined by single X-ray crystallography to study the ring size effect of the oxazine ring on Se...N intramolecular interactions.
URI: http://dx.doi.org/10.1021/om049722f
http://dspace.library.iitb.ac.in/xmlui/handle/10054/3748
http://hdl.handle.net/10054/3748
ISSN: 0276-7333
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