Hit 57

Reference List

FARX(1); FLST(1); RX(6)

Reaction (1 of 1)
Reaction ID132180
Reactant BRN136380
Reactant5-allyl-benzo[1,3]dioxole
Product BRN163628
Product5-oxiranylmethyl-benzo[1,3]dioxole
No. of Reaction Details6

Reaction Details (1 of 1)
Reaction ClassificationPreparation
Reagentiodine; yellow mercury oxide; water containing diethyl ether
Other ConditionsBehandeln der entwaesserten Loesung mit Kaliumhydroxyd
CommentHandbook
Citation Pointer504055; Journal; Fourneau; Tiffeneau; COREAF; C.R.Hebd.Seances Acad.Sci.; 141; 1905; 662; COREAF; C.R.Hebd.Seances Acad.Sci.; 140; 1905; 1595;

Reaction Details (2 of 1)
Reaction ClassificationPreparation
Reagentiodine; mercury (II)-oxide
Other ConditionsSchuetteln der Loesung mit gepulvertem Kaliumhydroxyd
CommentHandbook
Citation Pointer506822; Journal; Mosettig; CHBEAM; Chem.Ber.; 62; 1929; 1274;

Reaction Details (3 of 1)
Reaction ClassificationPreparation
Reagentperoxybenzoic acid; chloroform
CommentHandbook
Citation Pointer531965; Journal; Noller; Kneeland; JACSAT; J.Amer.Chem.Soc.; 68; 1946; 201;516184; Journal; Schoepf; Salzer; JLACBF; Justus Liebigs Ann. Chem.; 544; 1940; 1, 20;

Reaction Details (4 of 1)
Reaction ClassificationPreparation
Yield77 percent (BRN=163628)
Reagent40percent H2O2
Catalystmethyltrioctylammonium tetrakis(oxodiperoxotungsto)phosphate (2a)
Solventbenzene
Time60 min
Temperature60
Citation Pointer5707661; Journal; An, Zhong-wei; D'Aloisio, Rino; Venturello, Carlo; SYNTBF; Synthesis; EN; 12; 1992; 1229-1231;

Reaction Details (5 of 1)
Reaction ClassificationPreparation
Yield77 percent (BRN=163628)
Reagentaq. H2O2, methyltrioctylammonium tetrakis(diperoxotungsto)phosphate
Solvent1,2-dichloro-ethane
Time105 min
Temperature60
Citation Pointer5700985; Journal; Venturello, Carlo; D'Aloiso, Rino; JOCEAH; J.Org.Chem.; EN; 53; 7; 1988; 1553-1557;

Reaction Details (6 of 1)
Reaction ClassificationPreparation
Yield80 percent (BRN=163628)
ReagentCH3CO3H
SolventCHCl3
Time72 hour(s)
Other ConditionsAmbient temperature
Citation Pointer5940347; Journal; Barreiro, Eliezer J.; Costa, Paulo R. R.; Barros, Perola Regina V. R.; Queiroz, Waldemir M.; JRMPDM; J.Chem.Res.Miniprint; EN; 4; 1982; 1142-1165;

Reference (1 of 7)
Citation Number504055
Document TypeJournal
AuthorsFourneau; Tiffeneau
CODENCOREAF; COREAF
Journal TitleC.R.Hebd.Seances Acad.Sci.; C.R.Hebd.Seances Acad.Sci.
(Series) Volume141; 140
Publication Year1905; 1905
Page662; 1595

Reference (2 of 7)
Citation Number506822
Document TypeJournal
AuthorsMosettig
CODENCHBEAM
Journal TitleChem.Ber.
(Series) Volume62
Publication Year1929
Page1274

Reference (3 of 7)
Citation Number516184
Document TypeJournal
AuthorsSchoepf; Salzer
CODENJLACBF
Journal TitleJustus Liebigs Ann. Chem.
(Series) Volume544
Publication Year1940
Page1, 20

Reference (4 of 7)
Citation Number531965
Document TypeJournal
AuthorsNoller; Kneeland
CODENJACSAT
Journal TitleJ.Amer.Chem.Soc.
(Series) Volume68
Publication Year1946
Page201

Reference (5 of 7)
Citation Number5700985
Document TypeJournal
AuthorsVenturello, Carlo; D'Aloiso, Rino
CODENJOCEAH
Journal TitleJ.Org.Chem.
Language CodeEN
(Series) Volume53
Number7
Publication Year1988
Page1553-1557

Reference (6 of 7)
Citation Number5707661
Document TypeJournal
AuthorsAn, Zhong-wei; D'Aloisio, Rino; Venturello, Carlo
CODENSYNTBF
Journal TitleSynthesis
Language CodeEN
Number12
Publication Year1992
Page1229-1231

Reference (7 of 7)
Citation Number5940347
Document TypeJournal
AuthorsBarreiro, Eliezer J.; Costa, Paulo R. R.; Barros, Perola Regina V. R.; Queiroz, Waldemir M.
CODENJRMPDM
Journal TitleJ.Chem.Res.Miniprint
Language CodeEN
Number4
Publication Year1982
Page1142-1165

Copyright 1988-2001 Beilstein Institut zur Foerderung der Chemischen Wissenschaften. All rights reserved.