Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sanseverino Antonio M."'
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 13, Iss 5, Pp 700-703 (2002)
The preparation of epoxides is efficiently achieved in mild conditions by reaction of alkenes with trichloroisocyanuric acid in aqueous acetone followed by treatment of the resulting chlorohydrin with aqueous KOH in ether / pentane.
Externí odkaz:
https://doaj.org/article/be3c3d014e3c4efdbb41af222155588b
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 11, Iss 4, Pp 381-386 (2000)
Cohalogenation of (R)-limonene and (R)-carvomenthene with I2/H2O/Cu(OAc)2·H 2O in aqueous dioxane followed by base treatment produced stereospecifically the corresponding trans-epoxides. Same methodology of cohalogenation applied to related monoterp
Externí odkaz:
https://doaj.org/article/ffb228a19a8340938a5b29065c502098
Publikováno v:
Journal of the Brazilian Chemical Society, Vol 12, Iss 5, Pp 685-687 (2001)
The reaction of several alkenes with 0.4 mol equiv. PBr3/SiO2 in dichloromethane at room temperature gave the alkyl bromides with Markovnikov regiospecificity in 50 - 100% yield and short reaction time. Isoprene at - 8 °C in these conditions gave 1-
Externí odkaz:
https://doaj.org/article/d7ad0736924746b6869cf1fa1cfbbc0c
Publikováno v:
Journal of the Brazilian Chemical Society v.11 n.4 2000
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Vol 11, Iss 4, Pp 381-386 (2000)
Journal of the Brazilian Chemical Society, Volume: 11, Issue: 4, Pages: 381-386, Published: AUG 2000
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Vol 11, Iss 4, Pp 381-386 (2000)
Journal of the Brazilian Chemical Society, Volume: 11, Issue: 4, Pages: 381-386, Published: AUG 2000
Cohalogenation of (R)-limonene and (R)-carvomenthene with I2/H2O/Cu(OAc)2·H 2O in aqueous dioxane followed by base treatment produced stereospecifically the corresponding trans-epoxides. Same methodology of cohalogenation applied to related monoterp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8c6efa162e918df289df38c4195693df
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400010
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000400010
Publikováno v:
Phosphorus, Sulfur & Silicon & the Related Elements; Jun2004, Vol. 179 Issue 6, p1203-1208, 6p, 2 Diagrams, 1 Chart
Publikováno v:
Synthesis; November 1998, Vol. 1998 Issue: 11 p1584-1586, 3p
Publikováno v:
ChemInform; Jul2004, Vol. 35 Issue 29, pno-no, 1p