134309-95-8Relevant articles and documents
Reaction of tetrahydropyranyl azides with 5-R-bicyclo[2.2.1]-2-heptenes
Vasil'eva,Abzalov,Safarov
, p. 778 - 782 (1997)
The reaction of 5-R-bicyclo[2.2.1]-2-heptenes with 3-azido-4-hydroxy-4-methyltetrahydropyran and 4-azidomethyl-4-hydroxytetrahydropyran, obtained by opening the oxirane ring in epoxytetrahydropyrans with sodium azide, leads to the formation of N-tetrahydropyranylaziridines with 100% stereoselectivity. 1998 Plenum Publishing Corporation.
Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by np y5 receptor
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Page 53, (2010/02/05)
Compounds of formula (I): wherein: X is a group of formula (A) or (B): and R1, R2, R3, R4, n, x, y and z are as defined within are described. Processes for their preparation and their use in the treatment of disorders mediated by the neuropeptide Y5 receptor in a warm-blooded animal, such as a human being are also described.
Substituted alkenediols by alkylative double ring opening of dihydrofuran and dihydropyran epoxides
Hodgson, David M.,Stent, Matthew A. H.,Wilson, Francis X.
, p. 3401 - 3403 (2007/10/03)
Equation presented Dihydrofuran and dihydropyran epoxides undergo alkylative double ring opening with organolithiums to provide a new route to substituted alkenediols.