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1261345

ON=C1CCc2cc(Br)ccc2C1
Reaction #60356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCN(C2CCc3cc(Br)ccc3C2)CC1
Reaction #68901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1Br)CCC(=O)C2(C)C
Reaction #90058
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1Br)Cc1c([nH]c3cc(C#N)ccc13)C2(C)C
Reaction #90059
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1Br)Cc1c([nH]c3cc(Br)ccc13)C2(C)C.COc1cc2c(cc1Br)Cc1c([nH]c3cccc(Br)c13)C2(C)C
Reaction #90060
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1Br)C(=O)c1c([nH]c3cc(Cl)ccc13)C2(C)C
Reaction #90102
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cc2c(cc1OC)C(C)(C)C(=O)CC2
Reaction #90169
title compound
Ausbeute 430.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCc1ccc2c(c1)CCC(=O)C2
Reaction #172995
DOI: 10.1039/C8SC04228D
O=C(c1ccc2c(c1)CCC(NCc1ccccc1)C2)N1CCCC1CN1CCCC1
Reaction #194648
DOI: 10.1039/C8SC04228D
O=C(Cl)Cc1ccc(Br)cc1
Reaction #215693
4-bromo-phenylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)CCC(N1CCOCC1)C2)N1CCCC1CN1CCCC1
Reaction #228325
DOI: 10.1039/C8SC04228D
N#Cc1ccc2c(c1)CCC(=O)C2
Reaction #229517
DOI: 10.1039/C8SC04228D
O=C1CCc2cc(Br)ccc2C1
Reaction #377423
DOI: 10.1039/C8SC04228D
ON=C1CCc2cc(Br)ccc2C1
Reaction #383265
DOI: 10.1039/C8SC04228D
CCCC(NC1CCc2cc(Br)ccc2C1)C(=O)Nc1cn(C(C)(C)CN2CCCC2)cn1
Reaction #398930
DOI: 10.1039/C8SC04228D
Brc1ccc2c(c1)CCC1(C2)OCCO1
Reaction #444494
6-bromo-2-tetralone ethylene ketal
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)CCC1(C2)OCCO1
Reaction #457444
6-bromo-2-tetralone ethylene ketal
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)Cc1ccc(Br)cc1
Reaction #462448
4-bromophenylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2cc(Br)ccc2C1
Reaction #468722
6-bromo-2-tetralone
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)CCc1ncccc1-2
Reaction #542515
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
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