19740-75-1Relevant articles and documents
Haufe,G. et al.
, p. 575 - 585 (1978)
An Improved Preparation of 9-Oxabicyclonona-2,6-diene
Eaton, Philip E.,Millikan, Randall
, p. 483 - 484 (2007/10/02)
A useful procedure for the synthesis of 9-oxabicyclonona-2,6-diene free of isomers is provided.
Oxidation of Selenides and Tellurides with Positive Halogenating Species
Detty, Michael R.
, p. 274 - 279 (2007/10/02)
Treatment of diaryl or alkyl aryl selenides and diaryl or dialkyl tellurides first with a positive halogen source (N-chlorosuccinimide, tert-butyl hypochlorite) followed by alkaline hydrolysis (10percent sodium hydroxide, saturated sodium bicarbonate) gave the corresponding selenoxides or telluroxides (or hydrates) in good yield.The method is tolerant of a variety of functional groups including esters, olefins, alcohols, ethers, and ketones.The formal oxidation step is believed to be the formation of a chloroselenonium or chlorotelluronium species followed by hydrolysis. 1H NMR evidence is given for a benzylphenylselenonium species. Selenoxide fragmentation reactions during the hydrolysis step were observed