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CC(C)(C)OC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #176486
DOI: 10.1039/C8SC04228D
COc1cc(Br)ccc1OC1CNC1
Reaction #252008
DOI: 10.1039/C8SC04228D
COc1cc(Br)ccc1OC1CN(C2CCC2)C1
Reaction #276196
DOI: 10.1039/C8SC04228D
O=C(Cl)N1CC(Oc2ccc(Br)cc2)C1
Reaction #279691
DOI: 10.1039/C8SC04228D
NC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #294617
DOI: 10.1039/C8SC04228D
CNC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #404492
DOI: 10.1039/C8SC04228D
O=C(N1CCN(Cc2ccccc2)CC1)N1CC(Oc2ccc(Br)cc2)C1
Reaction #405821
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #425417
tert-butyl 3-(4-bromophenoxy)azetidine-1-carboxylate
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(OC2CNC2)cc1
Reaction #425418
3-(4-bromophenoxy)azetidine
Ausbeute 100.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #425419
1-[3-(4-bromophenoxy)azetidin-1-yl]ethanone
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)ccc1OC1CNC1
Reaction #642049
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)ccc1OC1CN(C2CCC2)C1
Reaction #642050
title compound
Ausbeute 56.6%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #906852
DOI: 10.1039/C8SC04228D
C#CCNC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1022829
DOI: 10.1039/C8SC04228D
O=C(N1CCN(c2ccccc2)CC1)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1045962
DOI: 10.1039/C8SC04228D
Brc1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #1061722
white crystals
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1061725
white granular crystals
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCNC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1061799
white crystals
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1061800
fine white crystals
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N1CC(Oc2ccc(Br)cc2)C1
Reaction #1061801
fine white crystals
Ausbeute 85.9%DOI: 10.6084/m9.figshare.5104873.v1
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